Canonical Allele Identifier: CA595579

Gene: MTHFR

Linked Data

• ClinVar Variation Id: 2907917
• ClinVar RCV Id: RCV003636772
• dbSNP Id: rs772698730
• ExAC: 1:11856365 G / T
• gnomAD v2: 1-11856365-G-T
• gnomAD v3: 1-11796308-G-T
• gnomAD v4: 1-11796308-G-T
• MyVariant Identifiers: chr1:g.11856365G>T (hg19) ; chr1:g.11796308G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11796308G>T , CM000663.2:g.11796308G>T	GRCh38
NC_000001.10:g.11856365G>T , CM000663.1:g.11856365G>T	GRCh37
NC_000001.9:g.11778952G>T	NCBI36
NG_013351.1:g.14796C>A , LRG_726:g.14796C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.678C>A	ENSP00000365669.3:p.Ile226=
ENST00000376585.6:c.801C>A	ENSP00000365770.1:p.Ile267=
ENST00000376590.9:c.678C>A MANE Select	ENSP00000365775.3:p.Ile226=
ENST00000376592.6:c.678C>A	ENSP00000365777.1:p.Ile226=
ENST00000423400.7:c.798C>A	ENSP00000398908.3:p.Ile266=
ENST00000641407.1:c.678C>A	ENSP00000493098.1:p.Ile226=
ENST00000641446.1:c.678C>A	ENSP00000493262.1:p.Ile226=
ENST00000641721.1:n.644-960C>A
ENST00000641747.1:c.*190C>A	ENSP00000493116.1:n.*190C>A
ENST00000641759.1:n.813C>A
ENST00000641805.1:n.961C>A
ENST00000641820.1:c.-58C>A	ENSP00000492937.1:n.-58C>A
ENST00000376583.7:c.801C>A	ENSP00000365767.3:p.Ile267=
ENST00000376585.5:c.801C>A	ENSP00000365770.1:p.Ile267=
ENST00000376590.7:c.678C>A	ENSP00000365775.3:p.Ile226=
ENST00000376592.5:c.678C>A	ENSP00000365777.1:p.Ile226=
NM_005957.4:c.678C>A , LRG_726t1:c.678C>A	NP_005948.3:p.Ile226=
XM_005263458.2:c.801C>A	XP_005263515.1:p.Ile267=
XM_005263460.3:c.678C>A	XP_005263517.1:p.Ile226=
XM_005263461.3:c.678C>A	XP_005263518.1:p.Ile226=
XM_005263462.3:c.678C>A	XP_005263519.1:p.Ile226=
XM_005263463.2:c.432C>A	XP_005263520.1:p.Ile144=
XM_011541495.1:c.798C>A	XP_011539797.1:p.Ile266=
XM_011541496.1:c.801C>A	XP_011539798.1:p.Ile267=
NM_001330358.1:c.801C>A	NP_001317287.1:p.Ile267=
XM_005263460.5:c.678C>A	XP_005263517.1:p.Ile226=
XM_005263462.4:c.678C>A	XP_005263519.1:p.Ile226=
XM_005263463.4:c.432C>A	XP_005263520.1:p.Ile144=
XM_011541495.3:c.798C>A	XP_011539797.1:p.Ile266=
XM_011541496.3:c.801C>A	XP_011539798.1:p.Ile267=
XM_017001328.2:c.801C>A	XP_016856817.1:p.Ile267=
XM_024447198.1:c.432C>A	XP_024302966.1:p.Ile144=
XR_002956640.1:n.1545C>A
NM_005957.5:c.678C>A MANE Select	NP_005948.3:p.Ile226=
NM_001330358.2:c.801C>A	NP_001317287.1:p.Ile267=