Canonical Allele Identifier: CA1740470091
Gene:

Linked Data

dbSNP Id: rs1795645711

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306283C>T , CM000669.2:g.124306283C>T GRCh38
NC_000007.13:g.123946337C>T , CM000669.1:g.123946337C>T GRCh37
NC_000007.12:g.123733573C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-195C>T