Canonical Allele Identifier: CA2614627976
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67491135-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491135G>T , CM000673.2:g.67491135G>T GRCh38
NC_000011.9:g.67258606G>T , CM000673.1:g.67258606G>T GRCh37
NC_000011.8:g.67015182G>T NCBI36
NG_008969.1:g.13102G>T , LRG_460:g.13102G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*142G>T ENSP00000507961.1:n.*142G>T
Search 100 bp 5'
Search 100 bp 3'