Canonical Allele Identifier: CA344080
Gene: AIP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 41169
ClinVar RCV Id: RCV000034068
dbSNP Id: rs104895072

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67487155G>T , CM000673.2:g.67487155G>T GRCh38
NC_000011.9:g.67254626G>T , CM000673.1:g.67254626G>T GRCh37
NC_000011.8:g.67011202G>T NCBI36
NG_008969.1:g.9122G>T , LRG_460:g.9122G>T

Transcript Alleles

HGVS Amino-acid change
NM_001302959.1:c.72G>T VV NP_001289888.1:p.Gly24=
NM_001302960.1:c.249G>T VV NP_001289889.1:p.Gly83=
NM_003977.3:c.249G>T VV NP_003968.3:p.Gly83=
XM_024448761.1:c.249G>T XP_024304529.1:p.Gly83=
NM_003977.4:c.249G>T VV MANE Preferred NP_003968.3:p.Gly83=
ENST00000279146.7:c.249G>T ENSP00000279146.3:p.Gly83=
ENST00000528641.6:c.249G>T ENSP00000434982.2:p.Gly83=
ENST00000529797.1:n.359G>T