Canonical Allele Identifier: CA679490435
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs1298793231
gnomAD v3: 11-67482977-G-A
gnomAD v4: 11-67482977-G-A
MyVariant Identifiers: chr11:g.67250448G>A (hg19) chr11:g.67482977G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482977G>A , CM000673.2:g.67482977G>A GRCh38
NC_000011.9:g.67250448G>A , CM000673.1:g.67250448G>A GRCh37
NC_000011.8:g.67007024G>A NCBI36
NG_008969.1:g.4944G>A , LRG_460:g.4944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-182G>A ENSP00000507935.1:n.-182G>A
XM_024448761.1:c.-182G>A XP_024304529.1:n.-182G>A
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