Canonical Allele Identifier: CA348473519

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138771452C>G (hg19) ; chr2:g.138013882C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013882C>G , CM000664.2:g.138013882C>G	GRCh38
NC_000002.11:g.138771452C>G , CM000664.1:g.138771452C>G	GRCh37
NC_000002.10:g.138487922C>G	NCBI36
NG_012966.1:g.54645C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.631C>G MANE Select	ENSP00000280097.3:p.Leu211Val
ENST00000280097.4:c.631C>G	ENSP00000280097.3:p.Leu211Val
ENST00000410115.5:c.631C>G	ENSP00000386940.1:p.Leu211Val
ENST00000485653.1:n.563C>G
NM_006895.2:c.631C>G	NP_008826.1:p.Leu211Val
XM_011511063.1:c.529C>G	XP_011509365.1:p.Leu177Val
XM_011511064.1:c.253C>G	XP_011509366.1:p.Leu85Val
XM_011511064.2:c.253C>G	XP_011509366.1:p.Leu85Val
XM_017003948.1:c.529C>G	XP_016859437.1:p.Leu177Val
XR_001739719.1:n.232-6086G>C
XR_002959286.1:n.1018C>G
NM_006895.3:c.631C>G MANE Select	NP_008826.1:p.Leu211Val