Canonical Allele Identifier: CA2614618015
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67483034-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483034G>T , CM000673.2:g.67483034G>T GRCh38
NC_000011.9:g.67250505G>T , CM000673.1:g.67250505G>T GRCh37
NC_000011.8:g.67007081G>T NCBI36
NG_008969.1:g.5001G>T , LRG_460:g.5001G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682699.1:c.-125G>T ENSP00000507935.1:n.-125G>T
ENST00000279146.8:c.-125G>T MANE Select ENSP00000279146.3:n.-125G>T
NM_001302960.1:c.-125G>T NP_001289889.1:n.-125G>T
NM_003977.3:c.-125G>T NP_003968.3:n.-125G>T
XM_024448761.1:c.-125G>T XP_024304529.1:n.-125G>T
NM_003977.4:c.-125G>T MANE Select NP_003968.3:n.-125G>T
NM_001302960.2:c.-125G>T NP_001289889.1:n.-125G>T
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