Canonical Allele Identifier: CA294176550

Gene: AANAT

Linked Data

• dbSNP Id: rs927479722
• gnomAD v3: 17-76467317-C-T
• gnomAD v4: 17-76467317-C-T
• MyVariant Identifiers: chr17:g.74463399C>T (hg19) ; chr17:g.76467317C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76467317C>T , CM000679.2:g.76467317C>T	GRCh38
NC_000017.10:g.74463399C>T , CM000679.1:g.74463399C>T	GRCh37
NC_000017.9:g.71974994C>T	NCBI36
NG_015976.1:g.18967C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000250615.7:c.60+1085C>T	ENSP00000250615.2:n.60+1085C>T
NM_001166579.1:c.60+1085C>T	NP_001160051.1:n.60+1085C>T
XM_011524415.1:c.-75-1355C>T	XP_011522717.1:n.-75-1355C>T
XM_011524416.1:c.133-1355C>T	XP_011522718.1:n.133-1355C>T
XM_011524417.1:c.133-1355C>T	XP_011522719.1:n.133-1355C>T
XM_011524418.1:c.133-1355C>T	XP_011522720.1:n.133-1355C>T
XM_011524419.1:c.133-1355C>T	XP_011522721.1:n.133-1355C>T
XM_011524420.1:c.133-1355C>T	XP_011522722.1:n.133-1355C>T
XM_011524421.1:c.133-1355C>T	XP_011522723.1:n.133-1355C>T
XM_011524422.1:c.16-1355C>T	XP_011522724.1:n.16-1355C>T
XM_011524423.1:c.-76+1006C>T	XP_011522725.1:n.-76+1006C>T
XM_017024259.1:c.-1316C>T	XP_016879748.1:n.-1316C>T
NM_001166579.2:c.60+1085C>T	NP_001160051.1:n.60+1085C>T