Canonical Allele Identifier: CA1648334846
Gene:

Linked Data

dbSNP Id: rs1768235764

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.95519472A>G , CM000668.2:g.95519472A>G GRCh38
NC_000006.11:g.95967348A>G , CM000668.1:g.95967348A>G GRCh37
NC_000006.10:g.96074069A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942795.1:n.94T>C