Canonical Allele Identifier: CA2713400316
Gene:

Linked Data

dbSNP Id: rs2115164407

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627232C>T , CM000668.2:g.151627232C>T GRCh38
NC_000006.11:g.151948367C>T , CM000668.1:g.151948367C>T GRCh37
NC_000006.10:g.151990060C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.658C>T
XR_943115.1:n.658C>T