Canonical Allele Identifier: CA2614617892
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67483016-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483016C>G , CM000673.2:g.67483016C>G GRCh38
NC_000011.9:g.67250487C>G , CM000673.1:g.67250487C>G GRCh37
NC_000011.8:g.67007063C>G NCBI36
NG_008969.1:g.4983C>G , LRG_460:g.4983C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-143C>G ENSP00000507935.1:n.-143C>G
XM_024448761.1:c.-143C>G XP_024304529.1:n.-143C>G
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