Canonical Allele Identifier: CA2749022110
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844025T>G , CM000664.2:g.17844025T>G GRCh38
NC_000002.11:g.18025292T>G , CM000664.1:g.18025292T>G GRCh37
NC_000002.10:g.17888773T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3669A>C