Canonical Allele Identifier: CA2614617905
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67483020-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483020C>A , CM000673.2:g.67483020C>A GRCh38
NC_000011.9:g.67250491C>A , CM000673.1:g.67250491C>A GRCh37
NC_000011.8:g.67007067C>A NCBI36
NG_008969.1:g.4987C>A , LRG_460:g.4987C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-139C>A ENSP00000507935.1:n.-139C>A
XM_024448761.1:c.-139C>A XP_024304529.1:n.-139C>A
Search 100 bp 5'
Search 100 bp 3'