Canonical Allele Identifier: CA224160600

Gene: AIP

Linked Data

• dbSNP Id: rs374248735
• gnomAD v4: 11-67482972-C-G
• MyVariant Identifiers: chr11:g.67250443C>G (hg19) ; chr11:g.67482972C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67482972C>G , CM000673.2:g.67482972C>G	GRCh38
NC_000011.9:g.67250443C>G , CM000673.1:g.67250443C>G	GRCh37
NC_000011.8:g.67007019C>G	NCBI36
NG_008969.1:g.4939C>G , LRG_460:g.4939C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682699.1:c.-187C>G	ENSP00000507935.1:n.-187C>G
XM_024448761.1:c.-187C>G	XP_024304529.1:n.-187C>G