Canonical Allele Identifier: CA1261549160
Gene:

Linked Data

dbSNP Id: rs1686250233

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74712000C>G , CM000664.2:g.74712000C>G GRCh38
NC_000002.11:g.74939127C>G , CM000664.1:g.74939127C>G GRCh37
NC_000002.10:g.74792635C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.313C>G