Canonical Allele Identifier: CA48266112
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11889995

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936272C>T , CM000664.2:g.51936272C>T GRCh38
NC_000002.11:g.52163410C>T , CM000664.1:g.52163410C>T GRCh37
NC_000002.10:g.52016914C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74784C>T
NR_135237.1:n.879+74784C>T