Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 11:47448924 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020757

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10262, 2010_April_001_284_RAPSN_601592_0002

This variation has 9 HGVS names - click the plus to show

11:g.47448924A>G
ENST00000352508.5:c.41T>C
ENSP00000298853.3:p.Leu14Pro
ENST00000298854.4:c.41T>C
ENSP00000298854.2:p.Leu14Pro
ENST00000529341.1:c.41T>C
ENSP00000431732.1:p.Leu14Pro
ENST00000524487.3:c.41T>C
ENSP00000435551.2:p.Leu14Pro

Variation displays