Canonical Allele Identifier: CA429193176

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138771352T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013782T>C , CM000664.2:g.138013782T>C	GRCh38
NC_000002.11:g.138771352T>C , CM000664.1:g.138771352T>C	GRCh37
NC_000002.10:g.138487822T>C	NCBI36
NG_012966.1:g.54545T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.531T>C MANE Select	ENSP00000280097.3:p.Ser177=
ENST00000280097.4:c.531T>C	ENSP00000280097.3:p.Ser177=
ENST00000410115.5:c.531T>C	ENSP00000386940.1:p.Ser177=
ENST00000485653.1:n.463T>C
NM_006895.2:c.531T>C	NP_008826.1:p.Ser177=
XM_011511063.1:c.429T>C	XP_011509365.1:p.Ser143=
XM_011511064.1:c.153T>C	XP_011509366.1:p.Ser51=
XM_011511064.2:c.153T>C	XP_011509366.1:p.Ser51=
XM_017003948.1:c.429T>C	XP_016859437.1:p.Ser143=
XR_001739719.1:n.232-5986A>G
XR_002959286.1:n.918T>C
NM_006895.3:c.531T>C MANE Select	NP_008826.1:p.Ser177=