Canonical Allele Identifier: CA1573962576
Gene:

Linked Data

dbSNP Id: rs1561760559

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113714882A>G , CM000667.2:g.113714882A>G GRCh38
NC_000005.9:g.113050579A>G , CM000667.1:g.113050579A>G GRCh37
NC_000005.8:g.113078478A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742840.1:n.153-18679A>G