Canonical Allele Identifier: CA1573933667
Gene:

Linked Data

dbSNP Id: rs1780062669

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660940C>G , CM000667.2:g.113660940C>G GRCh38
NC_000005.9:g.112996637C>G , CM000667.1:g.112996637C>G GRCh37
NC_000005.8:g.113024536C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27576C>G