Canonical Allele Identifier: CA337737954
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10436792

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13765774T>C , CM000686.2:g.13765774T>C GRCh38
NC_000024.9:g.15877654T>C , CM000686.1:g.15877654T>C GRCh37
NC_000024.8:g.14387048T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000430079.5:n.429+10985T>C
ENST00000460561.1:n.212+10985T>C
ENST00000472227.5:n.350+13769T>C