Canonical Allele Identifier: CA416362795

Gene: MTHFR

Linked Data

• dbSNP Id: rs1570474347
• gnomAD v4: 1-11794824-G-A
• MyVariant Identifiers: chr1:g.11854881G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11794824G>A , CM000663.2:g.11794824G>A	GRCh38
NC_000001.10:g.11854881G>A , CM000663.1:g.11854881G>A	GRCh37
NC_000001.9:g.11777468G>A	NCBI36
NG_013351.1:g.16280C>T , LRG_726:g.16280C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376585.6:c.1194C>T	ENSP00000365770.1:p.Arg398=
ENST00000376590.9:c.1071C>T MANE Select	ENSP00000365775.3:p.Arg357=
ENST00000376592.6:c.1071C>T	ENSP00000365777.1:p.Arg357=
ENST00000423400.7:c.1191C>T	ENSP00000398908.3:p.Arg397=
ENST00000641407.1:c.1071C>T	ENSP00000493098.1:p.Arg357=
ENST00000641446.1:c.1071C>T	ENSP00000493262.1:p.Arg357=
ENST00000641747.1:c.*583C>T	ENSP00000493116.1:n.*583C>T
ENST00000641759.1:n.1440C>T
ENST00000641805.1:n.1588C>T
ENST00000641820.1:c.336C>T	ENSP00000492937.1:p.Arg112=
ENST00000376583.7:c.1194C>T	ENSP00000365767.3:p.Arg398=
ENST00000376585.5:c.1194C>T	ENSP00000365770.1:p.Arg398=
ENST00000376590.7:c.1071C>T	ENSP00000365775.3:p.Arg357=
ENST00000376592.5:c.1071C>T	ENSP00000365777.1:p.Arg357=
NM_005957.4:c.1071C>T , LRG_726t1:c.1071C>T	NP_005948.3:p.Arg357=
XM_005263458.2:c.1194C>T	XP_005263515.1:p.Arg398=
XM_005263460.3:c.1071C>T	XP_005263517.1:p.Arg357=
XM_005263461.3:c.1071C>T	XP_005263518.1:p.Arg357=
XM_005263462.3:c.1071C>T	XP_005263519.1:p.Arg357=
XM_005263463.2:c.825C>T	XP_005263520.1:p.Arg275=
XM_011541495.1:c.1191C>T	XP_011539797.1:p.Arg397=
XM_011541496.1:c.1194C>T	XP_011539798.1:p.Arg398=
NM_001330358.1:c.1194C>T	NP_001317287.1:p.Arg398=
XM_005263460.5:c.1071C>T	XP_005263517.1:p.Arg357=
XM_005263462.4:c.1071C>T	XP_005263519.1:p.Arg357=
XM_005263463.4:c.825C>T	XP_005263520.1:p.Arg275=
XM_011541495.3:c.1191C>T	XP_011539797.1:p.Arg397=
XM_011541496.3:c.1194C>T	XP_011539798.1:p.Arg398=
XM_017001328.2:c.1194C>T	XP_016856817.1:p.Arg398=
XM_024447198.1:c.825C>T	XP_024302966.1:p.Arg275=
XR_002956640.1:n.2172C>T
NM_005957.5:c.1071C>T MANE Select	NP_005948.3:p.Arg357=
NM_001330358.2:c.1194C>T	NP_001317287.1:p.Arg398=