Canonical Allele Identifier: CA1258276520
Gene:

Linked Data

dbSNP Id: rs946378150

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637479T>C , CM000664.2:g.67637479T>C GRCh38
NC_000002.11:g.67864611T>C , CM000664.1:g.67864611T>C GRCh37
NC_000002.10:g.67718115T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13487A>G