Canonical Allele Identifier: CA13058051
Gene:

Linked Data

dbSNP Id: rs10818684

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122407651C>T , CM000671.2:g.122407651C>T GRCh38
NC_000009.11:g.125169930C>T , CM000671.1:g.125169930C>T GRCh37
NC_000009.10:g.124209751C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930325.1:n.211+871C>T
XR_930326.1:n.211+871C>T