Canonical Allele Identifier: CA1261549154
Gene:

Linked Data

dbSNP Id: rs1686250097

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711980A>C , CM000664.2:g.74711980A>C GRCh38
NC_000002.11:g.74939107A>C , CM000664.1:g.74939107A>C GRCh37
NC_000002.10:g.74792615A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.293A>C