Canonical Allele Identifier: CA224166253

Gene: AIP

Linked Data

• dbSNP Id: rs917928168
• gnomAD v3: 11-67491127-C-G
• gnomAD v4: 11-67491127-C-G
• MyVariant Identifiers: chr11:g.67258598C>G (hg19) ; chr11:g.67491127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67491127C>G , CM000673.2:g.67491127C>G	GRCh38
NC_000011.9:g.67258598C>G , CM000673.1:g.67258598C>G	GRCh37
NC_000011.8:g.67015174C>G	NCBI36
NG_008969.1:g.13094C>G , LRG_460:g.13094C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684657.1:c.*134C>G	ENSP00000507961.1:n.*134C>G