Canonical Allele Identifier: CA595239

Gene: MTHFR

Linked Data

• dbSNP Id: rs746327818
• ExAC: 1:11851275 T / C
• gnomAD v2: 1-11851275-T-C
• gnomAD v3: 1-11791218-T-C
• gnomAD v4: 1-11791218-T-C
• MyVariant Identifiers: chr1:g.11851275T>C (hg19) ; chr1:g.11791218T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11791218T>C , CM000663.2:g.11791218T>C	GRCh38
NC_000001.10:g.11851275T>C , CM000663.1:g.11851275T>C	GRCh37
NC_000001.9:g.11773862T>C	NCBI36
NG_013351.1:g.19886A>G , LRG_726:g.19886A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.1864A>G	ENSP00000365770.1:p.Met622Val
ENST00000376590.9:c.1741A>G MANE Select	ENSP00000365775.3:p.Met581Val
ENST00000376592.6:c.1741A>G	ENSP00000365777.1:p.Met581Val
ENST00000423400.7:c.1861A>G	ENSP00000398908.3:p.Met621Val
ENST00000641407.1:c.1741A>G	ENSP00000493098.1:p.Met581Val
ENST00000641446.1:c.*200A>G	ENSP00000493262.1:n.*200A>G
ENST00000641747.1:c.*1253A>G	ENSP00000493116.1:n.*1253A>G
ENST00000641759.1:n.2110A>G
ENST00000641805.1:n.2258A>G
ENST00000641820.1:c.1006A>G	ENSP00000492937.1:p.Met336Val
ENST00000376583.7:c.1864A>G	ENSP00000365767.3:p.Met622Val
ENST00000376585.5:c.1864A>G	ENSP00000365770.1:p.Met622Val
ENST00000376590.7:c.1741A>G	ENSP00000365775.3:p.Met581Val
ENST00000376592.5:c.1741A>G	ENSP00000365777.1:p.Met581Val
NM_005957.4:c.1741A>G , LRG_726t1:c.1741A>G	NP_005948.3:p.Met581Val
XM_005263458.2:c.1864A>G	XP_005263515.1:p.Met622Val
XM_005263460.3:c.1741A>G	XP_005263517.1:p.Met581Val
XM_005263461.3:c.1741A>G	XP_005263518.1:p.Met581Val
XM_005263462.3:c.1741A>G	XP_005263519.1:p.Met581Val
XM_005263463.2:c.1495A>G	XP_005263520.1:p.Met499Val
XM_011541495.1:c.1861A>G	XP_011539797.1:p.Met621Val
XM_011541496.1:c.1864A>G	XP_011539798.1:p.Met622Val
NM_001330358.1:c.1864A>G	NP_001317287.1:p.Met622Val
XM_005263460.5:c.1741A>G	XP_005263517.1:p.Met581Val
XM_005263462.4:c.1741A>G	XP_005263519.1:p.Met581Val
XM_005263463.4:c.1495A>G	XP_005263520.1:p.Met499Val
XM_011541495.3:c.1861A>G	XP_011539797.1:p.Met621Val
XM_011541496.3:c.1864A>G	XP_011539798.1:p.Met622Val
XM_017001328.2:c.1864A>G	XP_016856817.1:p.Met622Val
XM_024447198.1:c.1495A>G	XP_024302966.1:p.Met499Val
XR_002956640.1:n.2842A>G
NM_005957.5:c.1741A>G MANE Select	NP_005948.3:p.Met581Val
NM_001330358.2:c.1864A>G	NP_001317287.1:p.Met622Val