Canonical Allele Identifier: CA2661303283

Gene: HNMT

Linked Data

• gnomAD v4: 2-138013695-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013695T>G , CM000664.2:g.138013695T>G	GRCh38
NC_000002.11:g.138771265T>G , CM000664.1:g.138771265T>G	GRCh37
NC_000002.10:g.138487735T>G	NCBI36
NG_012966.1:g.54458T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.524-80T>G MANE Select	ENSP00000280097.3:n.524-80T>G
ENST00000280097.4:c.524-80T>G	ENSP00000280097.3:n.524-80T>G
ENST00000410115.5:c.524-80T>G	ENSP00000386940.1:n.524-80T>G
ENST00000485653.1:n.456-80T>G
NM_006895.2:c.524-80T>G	NP_008826.1:n.524-80T>G
XM_011511063.1:c.422-80T>G	XP_011509365.1:n.422-80T>G
XM_011511064.1:c.146-80T>G	XP_011509366.1:n.146-80T>G
XM_011511064.2:c.146-80T>G	XP_011509366.1:n.146-80T>G
XM_017003948.1:c.422-80T>G	XP_016859437.1:n.422-80T>G
XR_001739719.1:n.232-5899A>C
XR_002959286.1:n.911-80T>G
NM_006895.3:c.524-80T>G MANE Select	NP_008826.1:n.524-80T>G