Canonical Allele Identifier: CA15405513
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs4415084

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662413C>T , CM000667.2:g.44662413C>T GRCh38
NC_000005.9:g.44662515C>T , CM000667.1:g.44662515C>T GRCh37
NC_000005.8:g.44698272C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3856G>A
XR_925983.1:n.71-3856G>A