Canonical Allele Identifier: CA1035827819

Gene:

Linked Data

• dbSNP Id: rs1680371213
• gnomAD v3: 2-122883844-A-G
• gnomAD v4: 2-122883844-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122883844A>G , CM000664.2:g.122883844A>G	GRCh38
NC_000002.11:g.123641420A>G , CM000664.1:g.123641420A>G	GRCh37
NC_000002.10:g.123357890A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-1098A>G
XR_001739692.1:n.1451-1098A>G
XR_923292.2:n.1358-1098A>G