Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 7:30974052 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010308

Most severe consequence
Clinical significance

Synonyms

LSDB 2345

This variation has 12 HGVS names - click the plus to show

7:g.30974052C>A
ENST00000409904.4:c.473C>A
ENSP00000387113.3:p.Ala158Glu
ENST00000489974.2:n.438C>A
ENST00000337750.6:c.175-377C>A
ENST00000409316.2:c.51-377C>A
ENST00000461390.1:n.133C>A
ENST00000611037.1:c.111C>A
ENST00000396227.3:c.406-377C>A
ENST00000461424.2:n.241C>A
ENST00000326139.3:c.665C>A
ENSP00000320180.2:p.Ala222Glu

Variation displays