Canonical Allele Identifier: CA1672979227
Gene:

Linked Data

dbSNP Id: rs1777187993

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633684A>C , CM000668.2:g.151633684A>C GRCh38
NC_000006.11:g.151954819A>C , CM000668.1:g.151954819A>C GRCh37
NC_000006.10:g.151996512A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+3702A>C