Canonical Allele Identifier: CA995316559

Gene:

Linked Data

• dbSNP Id: rs1971155750
• gnomAD v3: 19-33522014-A-G
• gnomAD v4: 19-33522014-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33522014A>G , CM000681.2:g.33522014A>G	GRCh38
NC_000019.9:g.34012920A>G , CM000681.1:g.34012920A>G	GRCh37
NC_000019.8:g.38704760A>G	NCBI36
NG_013358.1:g.4880T>C
NG_013358.2:g.4880T>C

Transcript Alleles

HGVS	Amino-acid Change
XR_935918.1:n.73A>G
XR_935919.1:n.68A>G
XR_001754035.2:n.81A>G
XR_935918.2:n.81A>G