Canonical Allele Identifier: CA1704517753
Gene:

Linked Data

dbSNP Id: rs1784762302

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46032914T>C , CM000669.2:g.46032914T>C GRCh38
NC_000007.13:g.46072512T>C , CM000669.1:g.46072512T>C GRCh37
NC_000007.12:g.46039037T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745203.1:n.1270-3704T>C