Canonical Allele Identifier: CA756214989
Gene:

Linked Data

dbSNP Id: rs562123117

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884062A>G , CM000664.2:g.122884062A>G GRCh38
NC_000002.11:g.123641638A>G , CM000664.1:g.123641638A>G GRCh37
NC_000002.10:g.123358108A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-880A>G
XR_001739692.1:n.1451-880A>G
XR_923292.2:n.1358-880A>G