Canonical Allele Identifier: CA986411485

Gene: AANAT

Linked Data

• dbSNP Id: rs2073447341
• gnomAD v3: 17-76467187-C-G
• gnomAD v4: 17-76467187-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76467187C>G , CM000679.2:g.76467187C>G	GRCh38
NC_000017.10:g.74463269C>G , CM000679.1:g.74463269C>G	GRCh37
NC_000017.9:g.71974864C>G	NCBI36
NG_015976.1:g.18837C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250615.7:c.60+955C>G	ENSP00000250615.2:n.60+955C>G
NM_001166579.1:c.60+955C>G	NP_001160051.1:n.60+955C>G
XM_011524415.1:c.-75-1485C>G	XP_011522717.1:n.-75-1485C>G
XM_011524416.1:c.133-1485C>G	XP_011522718.1:n.133-1485C>G
XM_011524417.1:c.133-1485C>G	XP_011522719.1:n.133-1485C>G
XM_011524418.1:c.133-1485C>G	XP_011522720.1:n.133-1485C>G
XM_011524419.1:c.133-1485C>G	XP_011522721.1:n.133-1485C>G
XM_011524420.1:c.133-1485C>G	XP_011522722.1:n.133-1485C>G
XM_011524421.1:c.133-1485C>G	XP_011522723.1:n.133-1485C>G
XM_011524422.1:c.16-1485C>G	XP_011522724.1:n.16-1485C>G
XM_011524423.1:c.-76+876C>G	XP_011522725.1:n.-76+876C>G
XM_017024259.1:c.-1446C>G	XP_016879748.1:n.-1446C>G
NM_001166579.2:c.60+955C>G	NP_001160051.1:n.60+955C>G