Canonical Allele Identifier: CA340312
Gene: AIP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 4894
ClinVar RCV Id: RCV000005172
dbSNP Id: rs121908357

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483222C>T , CM000673.2:g.67483222C>T GRCh38
NC_000011.9:g.67250693C>T , CM000673.1:g.67250693C>T GRCh37
NC_000011.8:g.67007269C>T NCBI36
NG_008969.1:g.5189C>T , LRG_460:g.5189C>T

Transcript Alleles

HGVS Amino-acid change
NM_001302960.1:c.64C>T VV NP_001289889.1:p.Arg22Ter
NM_003977.3:c.64C>T VV NP_003968.3:p.Arg22Ter
XM_024448761.1:c.64C>T XP_024304529.1:p.Arg22Ter
NM_003977.4:c.64C>T VV MANE Preferred NP_003968.3:p.Arg22Ter
ENST00000279146.7:c.64C>T ENSP00000279146.3:p.Arg22Ter
ENST00000528641.6:c.64C>T ENSP00000434982.2:p.Arg22Ter
ENST00000529797.1:n.174C>T