Canonical Allele Identifier: CA1036161562
Gene:

Linked Data

dbSNP Id: rs1688786131

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431642C>T , CM000664.2:g.127431642C>T GRCh38
NC_000002.11:g.128189218C>T , CM000664.1:g.128189218C>T GRCh37
NC_000002.10:g.127905688C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+25G>A
XR_001739705.1:n.3607-3378G>A
XR_923313.2:n.4042+25G>A