Canonical Allele Identifier: CA1283487548
Gene:

Linked Data

dbSNP Id: rs17625845

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332155T>A , CM000664.2:g.120332155T>A GRCh38
NC_000002.11:g.121089731T>A , CM000664.1:g.121089731T>A GRCh37
NC_000002.10:g.120806201T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3349T>A XP_011510609.1:n.141+3349T>A