Canonical Allele Identifier: CA2485976200
Gene:

Linked Data

dbSNP Id: rs1658286971

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682246T>C , CM000663.2:g.213682246T>C GRCh38
NC_000001.10:g.213855589T>C , CM000663.1:g.213855589T>C GRCh37
NC_000001.9:g.211922212T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49171T>C
XR_001738464.1:n.426-49171T>C