Canonical Allele Identifier: CA429193177

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138771355C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013785C>A , CM000664.2:g.138013785C>A	GRCh38
NC_000002.11:g.138771355C>A , CM000664.1:g.138771355C>A	GRCh37
NC_000002.10:g.138487825C>A	NCBI36
NG_012966.1:g.54548C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.534C>A MANE Select	ENSP00000280097.3:p.Gly178=
ENST00000280097.4:c.534C>A	ENSP00000280097.3:p.Gly178=
ENST00000410115.5:c.534C>A	ENSP00000386940.1:p.Gly178=
ENST00000485653.1:n.466C>A
NM_006895.2:c.534C>A	NP_008826.1:p.Gly178=
XM_011511063.1:c.432C>A	XP_011509365.1:p.Gly144=
XM_011511064.1:c.156C>A	XP_011509366.1:p.Gly52=
XM_011511064.2:c.156C>A	XP_011509366.1:p.Gly52=
XM_017003948.1:c.432C>A	XP_016859437.1:p.Gly144=
XR_001739719.1:n.232-5989G>T
XR_002959286.1:n.921C>A
NM_006895.3:c.534C>A MANE Select	NP_008826.1:p.Gly178=