Canonical Allele Identifier: CA428913387

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138759674T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138002104T>C , CM000664.2:g.138002104T>C	GRCh38
NC_000002.11:g.138759674T>C , CM000664.1:g.138759674T>C	GRCh37
NC_000002.10:g.138476144T>C	NCBI36
NG_012966.1:g.42867T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.339T>C MANE Select	ENSP00000280097.3:p.Phe113=
ENST00000280097.4:c.339T>C	ENSP00000280097.3:p.Phe113=
ENST00000410115.5:c.339T>C	ENSP00000386940.1:p.Phe113=
ENST00000467390.5:n.351T>C
ENST00000485653.1:n.271T>C
NM_006895.2:c.339T>C	NP_008826.1:p.Phe113=
XM_011511063.1:c.237T>C	XP_011509365.1:p.Phe79=
XM_011511064.1:c.-40T>C	XP_011509366.1:n.-40T>C
XM_011511064.2:c.-40T>C	XP_011509366.1:n.-40T>C
XM_017003948.1:c.237T>C	XP_016859437.1:p.Phe79=
XM_017003949.2:c.339T>C	XP_016859438.1:p.Phe113=
XR_001739719.1:n.1039+4885A>G
XR_002959286.1:n.726T>C
NM_006895.3:c.339T>C MANE Select	NP_008826.1:p.Phe113=