Canonical Allele Identifier: CA1222435231
Gene:

Linked Data

dbSNP Id: rs1558226379

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491623A>G , CM000663.2:g.220491623A>G GRCh38
NC_000001.10:g.220664965A>G , CM000663.1:g.220664965A>G GRCh37
NC_000001.9:g.218731588A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-611A>G
XR_001737822.1:n.557-611A>G