Canonical Allele Identifier: CA620708634

Gene: ABCA17P

Linked Data

• dbSNP Id: rs1567360407 ; rs2141730259
• gnomAD v2: 16-2390760-AG-A
• gnomAD v3: 16-2340759-AG-A
• gnomAD v4: 16-2340759-AG-A
• MyVariant Identifiers: chr16:g.2390761del (hg19) ; chr16:g.2340760del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2340764del , CM000678.2:g.2340764del	GRCh38
NC_000016.9:g.2390765del , CM000678.1:g.2390765del	GRCh37
NC_000016.8:g.2330766del	NCBI36
NG_011790.1:g.4987del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000640929.1:n.42+1433del
ENST00000512848.5:n.182+1433del