Canonical Allele Identifier: CA2614628018
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67491141-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491141T>C , CM000673.2:g.67491141T>C GRCh38
NC_000011.9:g.67258612T>C , CM000673.1:g.67258612T>C GRCh37
NC_000011.8:g.67015188T>C NCBI36
NG_008969.1:g.13108T>C , LRG_460:g.13108T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*148T>C ENSP00000507961.1:n.*148T>C
Search 100 bp 5'
Search 100 bp 3'