Canonical Allele Identifier: CA1122156090

Gene:

Linked Data

• dbSNP Id: rs1823377936
• gnomAD v3: 9-21756013-A-G
• gnomAD v4: 9-21756013-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756013A>G , CM000671.2:g.21756013A>G	GRCh38
NC_000009.11:g.21756012A>G , CM000671.1:g.21756012A>G	GRCh37
NC_000009.10:g.21746012A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11812T>C