Canonical Allele Identifier: CA495970270
Gene: AGRP HGNC NCBI
ATP6V0D1-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67516671C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67482768C>T , CM000678.2:g.67482768C>T GRCh38
NC_000016.9:g.67516671C>T , CM000678.1:g.67516671C>T GRCh37
NC_000016.8:g.66074172C>T NCBI36
NG_011482.1:g.3419G>A
NG_011501.1:g.6046G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290953.3:c.267G>A (AGRP) MANE Select ENSP00000290953.3:p.Arg89=
ENST00000290953.2:c.267G>A (AGRP) ENSP00000290953.2:p.Arg89=
NM_001138.1:c.267G>A (AGRP) NP_001129.1:p.Arg89=
XM_011522927.1:c.267G>A (AGRP) XP_011521229.1:p.Arg89=
XR_243465.2:n.198+1249C>T (ATP6V0D1-DT)
XR_933690.1:n.199+1249C>T (ATP6V0D1-DT)
XR_933691.1:n.198+1249C>T (ATP6V0D1-DT)
XR_933692.1:n.200+1249C>T (ATP6V0D1-DT)
XR_001752246.1:n.193+1249C>T (ATP6V0D1-DT)
XR_001752247.1:n.193+1249C>T (ATP6V0D1-DT)
XR_001752248.1:n.195+1249C>T (ATP6V0D1-DT)
XR_001752249.1:n.193+1249C>T (ATP6V0D1-DT)
XR_001752250.1:n.193+1249C>T (ATP6V0D1-DT)
XR_933690.2:n.195+1249C>T (ATP6V0D1-DT)
XR_933691.2:n.201+1249C>T (ATP6V0D1-DT)
XR_933692.2:n.196+1249C>T (ATP6V0D1-DT)
NM_001138.2:c.267G>A (AGRP) MANE Select NP_001129.1:p.Arg89=