Canonical Allele Identifier: CA1122156108

Gene:

Linked Data

• dbSNP Id: rs539519295
• gnomAD v3: 9-21756089-C-G
• gnomAD v4: 9-21756089-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756089C>G , CM000671.2:g.21756089C>G	GRCh38
NC_000009.11:g.21756088C>G , CM000671.1:g.21756088C>G	GRCh37
NC_000009.10:g.21746088C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11736G>C