Canonical Allele Identifier: CA775172325

Gene: AANAT

Linked Data

• dbSNP Id: rs1374003113
• gnomAD v3: 17-76467467-A-C
• gnomAD v4: 17-76467467-A-C
• MyVariant Identifiers: chr17:g.74463549A>C (hg19) ; chr17:g.76467467A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76467467A>C , CM000679.2:g.76467467A>C	GRCh38
NC_000017.10:g.74463549A>C , CM000679.1:g.74463549A>C	GRCh37
NC_000017.9:g.71975144A>C	NCBI36
NG_015976.1:g.19117A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250615.7:c.61-1205A>C	ENSP00000250615.2:n.61-1205A>C
NM_001166579.1:c.61-1205A>C	NP_001160051.1:n.61-1205A>C
XM_011524415.1:c.-75-1205A>C	XP_011522717.1:n.-75-1205A>C
XM_011524416.1:c.133-1205A>C	XP_011522718.1:n.133-1205A>C
XM_011524417.1:c.133-1205A>C	XP_011522719.1:n.133-1205A>C
XM_011524418.1:c.133-1205A>C	XP_011522720.1:n.133-1205A>C
XM_011524419.1:c.133-1205A>C	XP_011522721.1:n.133-1205A>C
XM_011524420.1:c.133-1205A>C	XP_011522722.1:n.133-1205A>C
XM_011524421.1:c.133-1205A>C	XP_011522723.1:n.133-1205A>C
XM_011524422.1:c.16-1205A>C	XP_011522724.1:n.16-1205A>C
XM_011524423.1:c.-76+1156A>C	XP_011522725.1:n.-76+1156A>C
XM_017024259.1:c.-1166A>C	XP_016879748.1:n.-1166A>C
NM_001166579.2:c.61-1205A>C	NP_001160051.1:n.61-1205A>C