Canonical Allele Identifier: CA416119544

Gene: MTHFR

Linked Data

• dbSNP Id: rs2100493660
• MyVariant Identifiers: chr1:g.11850800C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790743C>T , CM000663.2:g.11790743C>T	GRCh38
NC_000001.10:g.11850800C>T , CM000663.1:g.11850800C>T	GRCh37
NC_000001.9:g.11773387C>T	NCBI36
NG_013351.1:g.20361G>A , LRG_726:g.20361G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.2031G>A	ENSP00000365770.1:p.Val677=
ENST00000376590.9:c.1908G>A MANE Select	ENSP00000365775.3:p.Val636=
ENST00000376592.6:c.1908G>A	ENSP00000365777.1:p.Val636=
ENST00000423400.7:c.2028G>A	ENSP00000398908.3:p.Val676=
ENST00000641407.1:c.1753-27G>A	ENSP00000493098.1:n.1753-27G>A
ENST00000641446.1:c.*367G>A	ENSP00000493262.1:n.*367G>A
ENST00000641747.1:c.*1420G>A	ENSP00000493116.1:n.*1420G>A
ENST00000641759.1:n.2277G>A
ENST00000641805.1:n.2270-27G>A
ENST00000641820.1:c.1173G>A	ENSP00000492937.1:p.Val391=
ENST00000376583.7:c.2031G>A	ENSP00000365767.3:p.Val677=
ENST00000376585.5:c.2031G>A	ENSP00000365770.1:p.Val677=
ENST00000376590.7:c.1908G>A	ENSP00000365775.3:p.Val636=
ENST00000376592.5:c.1908G>A	ENSP00000365777.1:p.Val636=
NM_005957.4:c.1908G>A , LRG_726t1:c.1908G>A	NP_005948.3:p.Val636=
XM_005263458.2:c.2031G>A	XP_005263515.1:p.Val677=
XM_005263460.3:c.1908G>A	XP_005263517.1:p.Val636=
XM_005263461.3:c.1908G>A	XP_005263518.1:p.Val636=
XM_005263462.3:c.1908G>A	XP_005263519.1:p.Val636=
XM_005263463.2:c.1662G>A	XP_005263520.1:p.Val554=
XM_011541495.1:c.2028G>A	XP_011539797.1:p.Val676=
XM_011541496.1:c.1876-27G>A	XP_011539798.1:n.1876-27G>A
NM_001330358.1:c.2031G>A	NP_001317287.1:p.Val677=
XM_005263460.5:c.1908G>A	XP_005263517.1:p.Val636=
XM_005263462.4:c.1908G>A	XP_005263519.1:p.Val636=
XM_005263463.4:c.1662G>A	XP_005263520.1:p.Val554=
XM_011541495.3:c.2028G>A	XP_011539797.1:p.Val676=
XM_011541496.3:c.1876-27G>A	XP_011539798.1:n.1876-27G>A
XM_017001328.2:c.1881G>A	XP_016856817.1:p.Val627=
XM_024447198.1:c.1662G>A	XP_024302966.1:p.Val554=
XR_002956640.1:n.2854-27G>A
NM_005957.5:c.1908G>A MANE Select	NP_005948.3:p.Val636=
NM_001330358.2:c.2031G>A	NP_001317287.1:p.Val677=