Canonical Allele Identifier: CA2614627855
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67491108-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491108A>G , CM000673.2:g.67491108A>G GRCh38
NC_000011.9:g.67258579A>G , CM000673.1:g.67258579A>G GRCh37
NC_000011.8:g.67015155A>G NCBI36
NG_008969.1:g.13075A>G , LRG_460:g.13075A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*115A>G ENSP00000507961.1:n.*115A>G
NM_001302959.1:c.*115A>G NP_001289888.1:n.*115A>G
NM_001302960.1:c.*248A>G NP_001289889.1:n.*248A>G
NM_003977.3:c.*115A>G NP_003968.3:n.*115A>G
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