Canonical Allele Identifier: CA15633104
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10761779

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.63515167A>G , CM000672.2:g.63515167A>G GRCh38
NC_000010.9:g.64944933A>G NCBI36
NC_000010.10:g.65274927A>G , CM000672.1:g.65274927A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000633035.1:n.113+6571T>C