Canonical Allele Identifier: CA246212058
Gene:

Linked Data

dbSNP Id: rs972448488

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529684T>C , CM000674.2:g.131529684T>C GRCh38
NC_000012.11:g.132014229T>C , CM000674.1:g.132014229T>C GRCh37
NC_000012.10:g.130580182T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+91A>G
XR_001749407.2:n.1067+91A>G