Canonical Allele Identifier: CA1481405791
Gene:

Linked Data

dbSNP Id: rs11944443

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499861A>T , CM000666.2:g.102499861A>T GRCh38
NC_000004.11:g.103421018A>T , CM000666.1:g.103421018A>T GRCh37
NC_000004.10:g.103640050A>T NCBI36
NG_050628.1:g.3533A>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1388T>A XP_011530769.1:n.643+1388T>A
NR_136202.1:n.48+2578T>A