Canonical Allele Identifier: CA2611999018

Gene:

Linked Data

• gnomAD v4: 11-2444555-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2444555C>T , CM000673.2:g.2444555C>T	GRCh38
NC_000011.9:g.2465785C>T , CM000673.1:g.2465785C>T	GRCh37
NC_000011.8:g.2422361C>T	NCBI36
NG_008935.1:g.4565C>T , LRG_287:g.4565C>T

Transcript Alleles

HGVS	Amino-acid Change
XR_930984.1:n.16G>A