Canonical Allele Identifier: CA599909934
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs1276253418
gnomAD v2: 11-67250460-C-A
gnomAD v3: 11-67482989-C-A
gnomAD v4: 11-67482989-C-A
MyVariant Identifiers: chr11:g.67250460C>A (hg19) chr11:g.67482989C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482989C>A , CM000673.2:g.67482989C>A GRCh38
NC_000011.9:g.67250460C>A , CM000673.1:g.67250460C>A GRCh37
NC_000011.8:g.67007036C>A NCBI36
NG_008969.1:g.4956C>A , LRG_460:g.4956C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-170C>A ENSP00000507935.1:n.-170C>A
XM_024448761.1:c.-170C>A XP_024304529.1:n.-170C>A
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