Canonical Allele Identifier: CA535800182
Gene:

Linked Data

dbSNP Id: rs1260199009

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883999C>T , CM000664.2:g.122883999C>T GRCh38
NC_000002.11:g.123641575C>T , CM000664.1:g.123641575C>T GRCh37
NC_000002.10:g.123358045C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-943C>T
XR_001739692.1:n.1451-943C>T
XR_923292.2:n.1358-943C>T