Canonical Allele Identifier: CA1286885904
Gene:

Linked Data

dbSNP Id: rs1573464662

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431565C>A , CM000664.2:g.127431565C>A GRCh38
NC_000002.11:g.128189141C>A , CM000664.1:g.128189141C>A GRCh37
NC_000002.10:g.127905611C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+102G>T
XR_001739705.1:n.3607-3301G>T
XR_923313.2:n.4042+102G>T