Canonical Allele Identifier: CA55082047
Gene:

Linked Data

dbSNP Id: rs756180530

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884083A>C , CM000664.2:g.122884083A>C GRCh38
NC_000002.11:g.123641659A>C , CM000664.1:g.123641659A>C GRCh37
NC_000002.10:g.123358129A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-859A>C
XR_001739692.1:n.1451-859A>C
XR_923292.2:n.1358-859A>C