Canonical Allele Identifier: CA224160584
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs745579152
gnomAD v4: 11-67482966-C-T
MyVariant Identifiers: chr11:g.67250437C>T (hg19) chr11:g.67482966C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482966C>T , CM000673.2:g.67482966C>T GRCh38
NC_000011.9:g.67250437C>T , CM000673.1:g.67250437C>T GRCh37
NC_000011.8:g.67007013C>T NCBI36
NG_008969.1:g.4933C>T , LRG_460:g.4933C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-193C>T ENSP00000507935.1:n.-193C>T
XM_024448761.1:c.-193C>T XP_024304529.1:n.-193C>T
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