Canonical Allele Identifier: CA348477802

Gene: HNMT

Linked Data

• MyVariant Identifiers: chr2:g.138759664A>C (hg19) ; chr2:g.138002094A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.138002094A>C , CM000664.2:g.138002094A>C	GRCh38
NC_000002.11:g.138759664A>C , CM000664.1:g.138759664A>C	GRCh37
NC_000002.10:g.138476134A>C	NCBI36
NG_012966.1:g.42857A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280097.5:c.329A>C MANE Select	ENSP00000280097.3:p.Asn110Thr
ENST00000280097.4:c.329A>C	ENSP00000280097.3:p.Asn110Thr
ENST00000410115.5:c.329A>C	ENSP00000386940.1:p.Asn110Thr
ENST00000467390.5:n.341A>C
ENST00000485653.1:n.261A>C
NM_006895.2:c.329A>C	NP_008826.1:p.Asn110Thr
XM_011511063.1:c.227A>C	XP_011509365.1:p.Asn76Thr
XM_011511064.1:c.-50A>C	XP_011509366.1:n.-50A>C
XM_011511064.2:c.-50A>C	XP_011509366.1:n.-50A>C
XM_017003948.1:c.227A>C	XP_016859437.1:p.Asn76Thr
XM_017003949.2:c.329A>C	XP_016859438.1:p.Asn110Thr
XR_001739719.1:n.1039+4895T>G
XR_002959286.1:n.716A>C
NM_006895.3:c.329A>C MANE Select	NP_008826.1:p.Asn110Thr