Canonical Allele Identifier: CA710128956
Gene:

Linked Data

dbSNP Id: rs1244791199

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612265A>G , CM000676.2:g.94612265A>G GRCh38
NC_000014.8:g.95078602A>G , CM000676.1:g.95078602A>G GRCh37
NC_000014.7:g.94148355A>G NCBI36
NG_012879.1:g.4889A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553947.1:c.805-32A>G