Canonical Allele Identifier: CA2753721059
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007003A>G , CM000664.2:g.195007003A>G GRCh38
NC_000002.11:g.195871727A>G , CM000664.1:g.195871727A>G GRCh37
NC_000002.10:g.195579972A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52432T>C