Canonical Allele Identifier: CA820839303

Gene:

Linked Data

• dbSNP Id: rs1190126093
• gnomAD v3: 6-151633777-C-A
• gnomAD v4: 6-151633777-C-A
• MyVariant Identifiers: chr6:g.151954912C>A (hg19) ; chr6:g.151633777C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633777C>A , CM000668.2:g.151633777C>A	GRCh38
NC_000006.11:g.151954912C>A , CM000668.1:g.151954912C>A	GRCh37
NC_000006.10:g.151996605C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943115.1:n.2496+3795C>A