Canonical Allele Identifier: CA150162798

Gene:

Linked Data

• dbSNP Id: rs971611476
• gnomAD v3: 6-151633442-A-G
• gnomAD v4: 6-151633442-A-G
• MyVariant Identifiers: chr6:g.151954577A>G (hg19) ; chr6:g.151633442A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633442A>G , CM000668.2:g.151633442A>G	GRCh38
NC_000006.11:g.151954577A>G , CM000668.1:g.151954577A>G	GRCh37
NC_000006.10:g.151996270A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3460A>G