Canonical Allele Identifier: CA338422206

Gene: MTHFR

Linked Data

• dbSNP Id: rs1018189670
• gnomAD v3: 1-11801190-C-A
• gnomAD v4: 1-11801190-C-A
• MyVariant Identifiers: chr1:g.11861247C>A (hg19) ; chr1:g.11801190C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801190C>A , CM000663.2:g.11801190C>A	GRCh38
NC_000001.10:g.11861247C>A , CM000663.1:g.11861247C>A	GRCh37
NC_000001.9:g.11783834C>A	NCBI36
NG_008766.1:g.41C>A
NG_013351.1:g.9914G>T , LRG_726:g.9914G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.446G>T	ENSP00000365669.3:p.Gly149Val
ENST00000376585.6:c.569G>T	ENSP00000365770.1:p.Gly190Val
ENST00000376590.9:c.446G>T MANE Select	ENSP00000365775.3:p.Gly149Val
ENST00000376592.6:c.446G>T	ENSP00000365777.1:p.Gly149Val
ENST00000423400.7:c.566G>T	ENSP00000398908.3:p.Gly189Val
ENST00000641407.1:c.446G>T	ENSP00000493098.1:p.Gly149Val
ENST00000641437.1:n.578G>T
ENST00000641446.1:c.446G>T	ENSP00000493262.1:p.Gly149Val
ENST00000641721.1:n.503G>T
ENST00000641747.1:c.237-868G>T	ENSP00000493116.1:n.237-868G>T
ENST00000641759.1:n.581G>T
ENST00000641805.1:n.729G>T
ENST00000641909.1:n.856G>T
ENST00000376583.7:c.569G>T	ENSP00000365767.3:p.Gly190Val
ENST00000376585.5:c.569G>T	ENSP00000365770.1:p.Gly190Val
ENST00000376590.7:c.446G>T	ENSP00000365775.3:p.Gly149Val
ENST00000376592.5:c.446G>T	ENSP00000365777.1:p.Gly149Val
NM_005957.4:c.446G>T , LRG_726t1:c.446G>T	NP_005948.3:p.Gly149Val
XM_005263458.2:c.569G>T	XP_005263515.1:p.Gly190Val
XM_005263460.3:c.446G>T	XP_005263517.1:p.Gly149Val
XM_005263461.3:c.446G>T	XP_005263518.1:p.Gly149Val
XM_005263462.3:c.446G>T	XP_005263519.1:p.Gly149Val
XM_005263463.2:c.200G>T	XP_005263520.1:p.Gly67Val
XM_011541495.1:c.566G>T	XP_011539797.1:p.Gly189Val
XM_011541496.1:c.569G>T	XP_011539798.1:p.Gly190Val
NM_001330358.1:c.569G>T	NP_001317287.1:p.Gly190Val
XM_005263460.5:c.446G>T	XP_005263517.1:p.Gly149Val
XM_005263462.4:c.446G>T	XP_005263519.1:p.Gly149Val
XM_005263463.4:c.200G>T	XP_005263520.1:p.Gly67Val
XM_011541495.3:c.566G>T	XP_011539797.1:p.Gly189Val
XM_011541496.3:c.569G>T	XP_011539798.1:p.Gly190Val
XM_017001328.2:c.569G>T	XP_016856817.1:p.Gly190Val
XM_024447198.1:c.200G>T	XP_024302966.1:p.Gly67Val
XR_002956640.1:n.1313G>T
NM_005957.5:c.446G>T MANE Select	NP_005948.3:p.Gly149Val
NM_001330358.2:c.569G>T	NP_001317287.1:p.Gly190Val