Canonical Allele Identifier: CA313334827

Gene: AHCY

Linked Data

• dbSNP Id: rs995016407
• gnomAD v2: 20-32857151-CG-C
• gnomAD v3: 20-34269345-CG-C
• gnomAD v4: 20-34269345-CG-C
• MyVariant Identifiers: chr20:g.32857152del (hg19) ; chr20:g.34269346del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34269346del , CM000682.2:g.34269346del	GRCh38
NC_000020.10:g.32857152del , CM000682.1:g.32857152del	GRCh37
NC_000020.9:g.32320813del	NCBI36
NG_011439.1:g.13982del

Transcript Alleles

HGVS	Amino-acid Change
XM_011528657.1:c.*7+11681del	XP_011526959.1:n.*7+11681del
XM_011528657.2:c.*7+11681del	XP_011526959.2:n.*7+11681del