Canonical Allele Identifier: CA2749638113
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534735A>G , CM000664.2:g.41534735A>G GRCh38
NC_000002.11:g.41761875A>G , CM000664.1:g.41761875A>G GRCh37
NC_000002.10:g.41615379A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+2991T>C
XR_939997.1:n.146+2991T>C
XR_939997.2:n.9529+2991T>C