Canonical Allele Identifier: CA2509009880
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67482980-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482980C>A , CM000673.2:g.67482980C>A GRCh38
NC_000011.9:g.67250451C>A , CM000673.1:g.67250451C>A GRCh37
NC_000011.8:g.67007027C>A NCBI36
NG_008969.1:g.4947C>A , LRG_460:g.4947C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-179C>A ENSP00000507935.1:n.-179C>A
XM_024448761.1:c.-179C>A XP_024304529.1:n.-179C>A
Search 100 bp 5'
Search 100 bp 3'