Canonical Allele Identifier: CA15173606
Gene:

Linked Data

dbSNP Id: rs17625845

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:n.141+3349T>C XP_011510609.1:p.=