Canonical Allele Identifier: CA1284436082
Gene:

Linked Data

dbSNP Id: rs1679097687

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379244C>A , CM000664.2:g.122379244C>A GRCh38
NC_000002.11:g.123136820C>A , CM000664.1:g.123136820C>A GRCh37
NC_000002.10:g.122853290C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-13719C>A
XR_001739684.1:n.556-13719C>A