Canonical Allele Identifier: CA2697867731
Gene:

Linked Data

dbSNP Id: rs1308605084

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682262C>A , CM000663.2:g.213682262C>A GRCh38
NC_000001.10:g.213855605C>A , CM000663.1:g.213855605C>A GRCh37
NC_000001.9:g.211922228C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49155C>A
XR_001738464.1:n.426-49155C>A