Canonical Allele Identifier: CA2749022108
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17843959T>C , CM000664.2:g.17843959T>C GRCh38
NC_000002.11:g.18025226T>C , CM000664.1:g.18025226T>C GRCh37
NC_000002.10:g.17888707T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3735A>G