Canonical Allele Identifier: CA292891016
Gene:

Linked Data

dbSNP Id: rs1003269921

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498402A>G , CM000679.2:g.63498402A>G GRCh38
NC_000017.10:g.61575763A>G , CM000679.1:g.61575763A>G GRCh37
NC_000017.9:g.58929495A>G NCBI36
NG_011648.1:g.26330A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1417A>G ENSP00000464149.1:n.1969+1417A>G