Canonical Allele Identifier: CA635306659

Gene: AHCY

Linked Data

• dbSNP Id: rs1267719256
• gnomAD v2: 20-32868016-CT-C
• gnomAD v4: 20-34280210-CT-C
• MyVariant Identifiers: chr20:g.32868017del (hg19) ; chr20:g.34280211del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34280211del , CM000682.2:g.34280211del	GRCh38
NC_000020.10:g.32868017del , CM000682.1:g.32868017del	GRCh37
NC_000020.9:g.32331678del	NCBI36
NG_012630.1:g.36592del
NG_012630.2:g.36592del

Transcript Alleles

HGVS	Amino-acid Change
XM_011528657.1:c.*7+816del	XP_011526959.1:n.*7+816del
XM_011528658.1:c.*7+816del	XP_011526960.1:n.*7+816del
XM_011528657.2:c.*7+816del	XP_011526959.2:n.*7+816del
XM_011528658.3:c.*7+816del	XP_011526960.2:n.*7+816del
XM_017027709.2:c.*7+816del	XP_016883198.1:n.*7+816del