Canonical Allele Identifier: CA1350284077
Gene:

Linked Data

dbSNP Id: rs1575062674

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207171G>C , CM000665.2:g.21207171G>C GRCh38
NC_000003.11:g.21248663G>C , CM000665.1:g.21248663G>C GRCh37
NC_000003.10:g.21223667G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3827G>C
XR_940646.2:n.547-3827G>C