Canonical Allele Identifier: CA1207463731
Gene:

Linked Data

dbSNP Id: rs1660425124

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741785A>G , CM000663.2:g.172741785A>G GRCh38
NC_000001.10:g.172710925A>G , CM000663.1:g.172710925A>G GRCh37
NC_000001.9:g.170977548A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-34034A>G