Canonical Allele Identifier: CA2614627845
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67491105-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491105C>T , CM000673.2:g.67491105C>T GRCh38
NC_000011.9:g.67258576C>T , CM000673.1:g.67258576C>T GRCh37
NC_000011.8:g.67015152C>T NCBI36
NG_008969.1:g.13072C>T , LRG_460:g.13072C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*112C>T ENSP00000507961.1:n.*112C>T
NM_001302959.1:c.*112C>T NP_001289888.1:n.*112C>T
NM_001302960.1:c.*245C>T NP_001289889.1:n.*245C>T
NM_003977.3:c.*112C>T NP_003968.3:n.*112C>T
Search 100 bp 5'
Search 100 bp 3'