Canonical Allele Identifier: CA1648334827
Gene:

Linked Data

dbSNP Id: rs1768235558

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.95519453C>T , CM000668.2:g.95519453C>T GRCh38
NC_000006.11:g.95967329C>T , CM000668.1:g.95967329C>T GRCh37
NC_000006.10:g.96074050C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942795.1:n.113G>A