Canonical Allele Identifier: CA8786576
Gene: AANAT HGNC NCBI

Linked Data

dbSNP Id: rs767271473

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469711A>G , CM000679.2:g.76469711A>G GRCh38
NC_000017.10:g.74465793A>G , CM000679.1:g.74465793A>G GRCh37
NC_000017.9:g.71977388A>G NCBI36
NG_015976.1:g.21361A>G
NG_032852.1:g.36717T>C , LRG_532:g.36717T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392492.8:c.365A>G MANE Select ENSP00000376282.2:p.His122Arg
ENST00000250615.7:c.500A>G ENSP00000250615.2:p.His167Arg
ENST00000392492.7:c.365A>G ENSP00000376282.2:p.His122Arg
ENST00000587798.1:c.*142A>G ENSP00000468239.1:n.*142A>G
NM_001088.2:c.365A>G NP_001079.1:p.His122Arg
NM_001166579.1:c.500A>G NP_001160051.1:p.His167Arg
NR_110548.1:n.676A>G
XM_011524415.1:c.365A>G XP_011522717.1:p.His122Arg
XM_011524416.1:c.572A>G XP_011522718.1:p.His191Arg
XM_011524417.1:c.572A>G XP_011522719.1:p.His191Arg
XM_011524418.1:c.572A>G XP_011522720.1:p.His191Arg
XM_011524419.1:c.572A>G XP_011522721.1:p.His191Arg
XM_011524420.1:c.572A>G XP_011522722.1:p.His191Arg
XM_011524421.1:c.572A>G XP_011522723.1:p.His191Arg
XM_011524422.1:c.455A>G XP_011522724.1:p.His152Arg
XM_011524423.1:c.365A>G XP_011522725.1:p.His122Arg
XM_017024259.1:c.479A>G XP_016879748.1:p.His160Arg
NM_001088.3:c.365A>G MANE Select NP_001079.1:p.His122Arg
NR_110548.2:n.621A>G
NM_001166579.2:c.500A>G NP_001160051.1:p.His167Arg