Canonical Allele Identifier: CA1036161548
Gene:

Linked Data

dbSNP Id: rs930843296

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431632G>T , CM000664.2:g.127431632G>T GRCh38
NC_000002.11:g.128189208G>T , CM000664.1:g.128189208G>T GRCh37
NC_000002.10:g.127905678G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+35C>A
XR_001739705.1:n.3607-3368C>A
XR_923313.2:n.4042+35C>A