Canonical Allele Identifier: CA15379874
Gene:

Linked Data

dbSNP Id: rs7709212

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159337169T>C , CM000667.2:g.159337169T>C GRCh38
NC_000005.9:g.158764177T>C , CM000667.1:g.158764177T>C GRCh37
NC_000005.8:g.158696755T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037889.1:n.745+4166T>C