Canonical Allele Identifier: CA338480998

Gene: MTHFR

Linked Data

• dbSNP Id: rs2100540622
• MyVariant Identifiers: chr1:g.11856417G>C (hg19) ; chr1:g.11796360G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796360G>C , CM000663.2:g.11796360G>C	GRCh38
NC_000001.10:g.11856417G>C , CM000663.1:g.11856417G>C	GRCh37
NC_000001.9:g.11779004G>C	NCBI36
NG_013351.1:g.14744C>G , LRG_726:g.14744C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376486.3:c.626C>G	ENSP00000365669.3:p.Ala209Gly
ENST00000376585.6:c.749C>G	ENSP00000365770.1:p.Ala250Gly
ENST00000376590.9:c.626C>G MANE Select	ENSP00000365775.3:p.Ala209Gly
ENST00000376592.6:c.626C>G	ENSP00000365777.1:p.Ala209Gly
ENST00000423400.7:c.746C>G	ENSP00000398908.3:p.Ala249Gly
ENST00000641407.1:c.626C>G	ENSP00000493098.1:p.Ala209Gly
ENST00000641446.1:c.626C>G	ENSP00000493262.1:p.Ala209Gly
ENST00000641721.1:n.644-1012C>G
ENST00000641747.1:c.*138C>G	ENSP00000493116.1:n.*138C>G
ENST00000641759.1:n.761C>G
ENST00000641805.1:n.909C>G
ENST00000641820.1:c.-110C>G	ENSP00000492937.1:n.-110C>G
ENST00000376583.7:c.749C>G	ENSP00000365767.3:p.Ala250Gly
ENST00000376585.5:c.749C>G	ENSP00000365770.1:p.Ala250Gly
ENST00000376590.7:c.626C>G	ENSP00000365775.3:p.Ala209Gly
ENST00000376592.5:c.626C>G	ENSP00000365777.1:p.Ala209Gly
NM_005957.4:c.626C>G , LRG_726t1:c.626C>G	NP_005948.3:p.Ala209Gly
XM_005263458.2:c.749C>G	XP_005263515.1:p.Ala250Gly
XM_005263460.3:c.626C>G	XP_005263517.1:p.Ala209Gly
XM_005263461.3:c.626C>G	XP_005263518.1:p.Ala209Gly
XM_005263462.3:c.626C>G	XP_005263519.1:p.Ala209Gly
XM_005263463.2:c.380C>G	XP_005263520.1:p.Ala127Gly
XM_011541495.1:c.746C>G	XP_011539797.1:p.Ala249Gly
XM_011541496.1:c.749C>G	XP_011539798.1:p.Ala250Gly
NM_001330358.1:c.749C>G	NP_001317287.1:p.Ala250Gly
XM_005263460.5:c.626C>G	XP_005263517.1:p.Ala209Gly
XM_005263462.4:c.626C>G	XP_005263519.1:p.Ala209Gly
XM_005263463.4:c.380C>G	XP_005263520.1:p.Ala127Gly
XM_011541495.3:c.746C>G	XP_011539797.1:p.Ala249Gly
XM_011541496.3:c.749C>G	XP_011539798.1:p.Ala250Gly
XM_017001328.2:c.749C>G	XP_016856817.1:p.Ala250Gly
XM_024447198.1:c.380C>G	XP_024302966.1:p.Ala127Gly
XR_002956640.1:n.1493C>G
NM_005957.5:c.626C>G MANE Select	NP_005948.3:p.Ala209Gly
NM_001330358.2:c.749C>G	NP_001317287.1:p.Ala250Gly