Canonical Allele Identifier: CA2571689980
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007208A>G , CM000664.2:g.195007208A>G GRCh38
NC_000002.11:g.195871932A>G , CM000664.1:g.195871932A>G GRCh37
NC_000002.10:g.195580177A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52227T>C