Canonical Allele Identifier: CA495969805
Gene: AGRP HGNC NCBI
ATP6V0D1-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67516569A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67482666A>C , CM000678.2:g.67482666A>C GRCh38
NC_000016.9:g.67516569A>C , CM000678.1:g.67516569A>C GRCh37
NC_000016.8:g.66074070A>C NCBI36
NG_011482.1:g.3521T>G
NG_011501.1:g.6148T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290953.3:c.369T>G (AGRP) MANE Select ENSP00000290953.3:p.Gly123=
ENST00000290953.2:c.369T>G (AGRP) ENSP00000290953.2:p.Gly123=
NM_001138.1:c.369T>G (AGRP) NP_001129.1:p.Gly123=
XM_011522927.1:c.369T>G (AGRP) XP_011521229.1:p.Gly123=
XR_243465.2:n.198+1147A>C (ATP6V0D1-DT)
XR_933690.1:n.199+1147A>C (ATP6V0D1-DT)
XR_933691.1:n.198+1147A>C (ATP6V0D1-DT)
XR_933692.1:n.200+1147A>C (ATP6V0D1-DT)
XR_001752246.1:n.193+1147A>C (ATP6V0D1-DT)
XR_001752247.1:n.193+1147A>C (ATP6V0D1-DT)
XR_001752248.1:n.195+1147A>C (ATP6V0D1-DT)
XR_001752249.1:n.193+1147A>C (ATP6V0D1-DT)
XR_001752250.1:n.193+1147A>C (ATP6V0D1-DT)
XR_933690.2:n.195+1147A>C (ATP6V0D1-DT)
XR_933691.2:n.201+1147A>C (ATP6V0D1-DT)
XR_933692.2:n.196+1147A>C (ATP6V0D1-DT)
NM_001138.2:c.369T>G (AGRP) MANE Select NP_001129.1:p.Gly123=