Canonical Allele Identifier: CA414966215
Gene: AMELY HGNC NCBI

Linked Data

dbSNP Id: rs1232350744
gnomAD v2: Y-6736087-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6868046C>G , CM000686.2:g.6868046C>G GRCh38
NC_000024.9:g.6736087C>G , CM000686.1:g.6736087C>G GRCh37
NC_000024.8:g.6796087C>G NCBI36
NG_008011.1:g.10982G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651267.2:c.564G>C MANE Select ENSP00000498344.1:p.Gln188His
ENST00000215479.10:c.564G>C ENSP00000215479.5:p.Gln188His
ENST00000651267.1:c.564G>C ENSP00000498344.1:p.Gln188His
ENST00000215479.9:c.564G>C ENSP00000215479.5:p.Gln188His
ENST00000383036.1:c.606G>C ENSP00000372505.1:p.Gln202His
NM_001143.1:c.564G>C NP_001134.1:p.Gln188His
XM_011531472.1:c.606G>C XP_011529774.1:p.Gln202His
NM_001364814.1:c.606G>C NP_001351743.1:p.Gln202His
NM_001143.2:c.564G>C MANE Select NP_001134.1:p.Gln188His