Canonical Allele Identifier: CA1358881705
Gene:

Linked Data

dbSNP Id: rs1575204342

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263204C>T , CM000665.2:g.39263204C>T GRCh38
NC_000003.11:g.39304695C>T , CM000665.1:g.39304695C>T GRCh37
NC_000003.10:g.39279699C>T NCBI36
NG_016362.1:g.23532G>A

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2721C>T