Canonical Allele Identifier: CA428913332

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138759653G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138002083G>T , CM000664.2:g.138002083G>T	GRCh38
NC_000002.11:g.138759653G>T , CM000664.1:g.138759653G>T	GRCh37
NC_000002.10:g.138476123G>T	NCBI36
NG_012966.1:g.42846G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.318G>T MANE Select	ENSP00000280097.3:p.Ser106=
ENST00000280097.4:c.318G>T	ENSP00000280097.3:p.Ser106=
ENST00000410115.5:c.318G>T	ENSP00000386940.1:p.Ser106=
ENST00000467390.5:n.330G>T
ENST00000485653.1:n.250G>T
NM_006895.2:c.318G>T	NP_008826.1:p.Ser106=
XM_011511063.1:c.216G>T	XP_011509365.1:p.Ser72=
XM_011511064.1:c.-61G>T	XP_011509366.1:n.-61G>T
XM_011511064.2:c.-61G>T	XP_011509366.1:n.-61G>T
XM_017003948.1:c.216G>T	XP_016859437.1:p.Ser72=
XM_017003949.2:c.318G>T	XP_016859438.1:p.Ser106=
XR_001739719.1:n.1039+4906C>A
XR_002959286.1:n.705G>T
NM_006895.3:c.318G>T MANE Select	NP_008826.1:p.Ser106=