Canonical Allele Identifier: CA2638676355

Gene:

Linked Data

• gnomAD v4: 17-50211911-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211911A>G , CM000679.2:g.50211911A>G	GRCh38
NC_000017.10:g.48289272A>G , CM000679.1:g.48289272A>G	GRCh37
NC_000017.9:g.45644271A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-1924A>G