Canonical Allele Identifier: CA2702244242
Gene:

Linked Data

dbSNP Id: rs764255650

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39263227C>T , CM000665.2:g.39263227C>T GRCh38
NC_000003.11:g.39304718C>T , CM000665.1:g.39304718C>T GRCh37
NC_000003.10:g.39279722C>T NCBI36
NG_016362.1:g.23509G>A

Transcript Alleles

HGVS Amino-acid change
XR_001740660.2:n.2744C>T