Canonical Allele Identifier: CA348473503

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138771450A>C (hg19) ; chr2:g.138013880A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138013880A>C , CM000664.2:g.138013880A>C	GRCh38
NC_000002.11:g.138771450A>C , CM000664.1:g.138771450A>C	GRCh37
NC_000002.10:g.138487920A>C	NCBI36
NG_012966.1:g.54643A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000280097.5:c.629A>C MANE Select	ENSP00000280097.3:p.Asn210Thr
ENST00000280097.4:c.629A>C	ENSP00000280097.3:p.Asn210Thr
ENST00000410115.5:c.629A>C	ENSP00000386940.1:p.Asn210Thr
ENST00000485653.1:n.561A>C
NM_006895.2:c.629A>C	NP_008826.1:p.Asn210Thr
XM_011511063.1:c.527A>C	XP_011509365.1:p.Asn176Thr
XM_011511064.1:c.251A>C	XP_011509366.1:p.Asn84Thr
XM_011511064.2:c.251A>C	XP_011509366.1:p.Asn84Thr
XM_017003948.1:c.527A>C	XP_016859437.1:p.Asn176Thr
XR_001739719.1:n.232-6084T>G
XR_002959286.1:n.1016A>C
NM_006895.3:c.629A>C MANE Select	NP_008826.1:p.Asn210Thr