Canonical Allele Identifier: CA495970192
Gene: AGRP HGNC NCBI
ATP6V0D1-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67516641C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67482738C>A , CM000678.2:g.67482738C>A GRCh38
NC_000016.9:g.67516641C>A , CM000678.1:g.67516641C>A GRCh37
NC_000016.8:g.66074142C>A NCBI36
NG_011482.1:g.3449G>T
NG_011501.1:g.6076G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000290953.3:c.297G>T (AGRP) MANE Select ENSP00000290953.3:p.Val99=
ENST00000290953.2:c.297G>T (AGRP) ENSP00000290953.2:p.Val99=
NM_001138.1:c.297G>T (AGRP) NP_001129.1:p.Val99=
XM_011522927.1:c.297G>T (AGRP) XP_011521229.1:p.Val99=
XR_243465.2:n.198+1219C>A (ATP6V0D1-DT)
XR_933690.1:n.199+1219C>A (ATP6V0D1-DT)
XR_933691.1:n.198+1219C>A (ATP6V0D1-DT)
XR_933692.1:n.200+1219C>A (ATP6V0D1-DT)
XR_001752246.1:n.193+1219C>A (ATP6V0D1-DT)
XR_001752247.1:n.193+1219C>A (ATP6V0D1-DT)
XR_001752248.1:n.195+1219C>A (ATP6V0D1-DT)
XR_001752249.1:n.193+1219C>A (ATP6V0D1-DT)
XR_001752250.1:n.193+1219C>A (ATP6V0D1-DT)
XR_933690.2:n.195+1219C>A (ATP6V0D1-DT)
XR_933691.2:n.201+1219C>A (ATP6V0D1-DT)
XR_933692.2:n.196+1219C>A (ATP6V0D1-DT)
NM_001138.2:c.297G>T (AGRP) MANE Select NP_001129.1:p.Val99=