Canonical Allele Identifier: CA1283591729
Gene:

Linked Data

dbSNP Id: rs1678952033

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120551847G>C , CM000664.2:g.120551847G>C GRCh38
NC_000002.11:g.121309423G>C , CM000664.1:g.121309423G>C GRCh37
NC_000002.10:g.121025893G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923262.1:n.1487+41C>G
XR_001739680.2:n.1495+41C>G
XR_001739681.2:n.2128+41C>G
XR_001739682.1:n.1495+41C>G
XR_002959417.1:n.1495+41C>G