Canonical Allele Identifier: CA937524944

Gene:

Linked Data

• dbSNP Id: rs1856778951
• gnomAD v3: 11-45506650-A-C
• gnomAD v4: 11-45506650-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506650A>C , CM000673.2:g.45506650A>C	GRCh38
NC_000011.9:g.45528200A>C , CM000673.1:g.45528200A>C	GRCh37
NC_000011.8:g.45484776A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16879T>G
XR_931245.3:n.566-16879T>G