Canonical Allele Identifier: CA337739488
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11096429

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13836385A>G , CM000686.2:g.13836385A>G GRCh38
NC_000024.8:g.14457659A>G NCBI36
NC_000024.9:g.15948265A>G , CM000686.1:g.15948265A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000430079.5:n.478-18059A>G
ENST00000460561.1:n.261-22132A>G
ENST00000472227.5:n.399-22117A>G