Canonical Allele Identifier: CA599909931
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs1340988359
gnomAD v2: 11-67250440-A-G
gnomAD v3: 11-67482969-A-G
gnomAD v4: 11-67482969-A-G
MyVariant Identifiers: chr11:g.67250440A>G (hg19) chr11:g.67482969A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482969A>G , CM000673.2:g.67482969A>G GRCh38
NC_000011.9:g.67250440A>G , CM000673.1:g.67250440A>G GRCh37
NC_000011.8:g.67007016A>G NCBI36
NG_008969.1:g.4936A>G , LRG_460:g.4936A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-190A>G ENSP00000507935.1:n.-190A>G
XM_024448761.1:c.-190A>G XP_024304529.1:n.-190A>G
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