Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 14:94844912 (forward strand) | View in location tab

Most severe consequence
Clinical significance

This variation has 18 HGVS names - click the plus to show

14:g.94844912T>A
ENST00000448921.1:c.1131A>T
ENSP00000416066.1:p.Leu377Phe
ENST00000449399.3:c.1131A>T
ENSP00000416354.3:p.Leu377Phe
ENST00000355814.4:c.1131A>T
ENSP00000348068.4:p.Leu377Phe
ENST00000404814.4:c.1131A>T
ENSP00000385960.4:p.Leu377Phe
ENST00000393088.4:c.1131A>T
ENSP00000376803.4:p.Leu377Phe
ENST00000393087.4:c.1131A>T
ENSP00000376802.4:p.Leu377Phe
ENST00000437397.1:c.1131A>T
ENSP00000408474.1:p.Leu377Phe
ENST00000489769.1:c.*430A>T
ENST00000440909.1:c.1131A>T
ENSP00000390299.1:p.Leu377Phe

Variation displays