Canonical Allele Identifier: CA416360095

Gene: MTHFR

Linked Data

• ClinVar Variation Id: 1573495
• ClinVar RCV Id: RCV002207967 ; RCV002372875
• dbSNP Id: rs1185978577
• gnomAD v2: 1-11861303-G-A
• gnomAD v4: 1-11801246-G-A
• MyVariant Identifiers: chr1:g.11861303G>A (hg19) ; chr1:g.11801246G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801246G>A , CM000663.2:g.11801246G>A	GRCh38
NC_000001.10:g.11861303G>A , CM000663.1:g.11861303G>A	GRCh37
NC_000001.9:g.11783890G>A	NCBI36
NG_008766.1:g.97G>A
NG_013351.1:g.9858C>T , LRG_726:g.9858C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376486.3:c.390C>T	ENSP00000365669.3:p.Cys130=
ENST00000376585.6:c.513C>T	ENSP00000365770.1:p.Cys171=
ENST00000376590.9:c.390C>T MANE Select	ENSP00000365775.3:p.Cys130=
ENST00000376592.6:c.390C>T	ENSP00000365777.1:p.Cys130=
ENST00000423400.7:c.510C>T	ENSP00000398908.3:p.Cys170=
ENST00000641407.1:c.390C>T	ENSP00000493098.1:p.Cys130=
ENST00000641437.1:n.522C>T
ENST00000641446.1:c.390C>T	ENSP00000493262.1:p.Cys130=
ENST00000641721.1:n.447C>T
ENST00000641747.1:c.237-924C>T	ENSP00000493116.1:n.237-924C>T
ENST00000641759.1:n.525C>T
ENST00000641805.1:n.673C>T
ENST00000641909.1:n.800C>T
ENST00000376583.7:c.513C>T	ENSP00000365767.3:p.Cys171=
ENST00000376585.5:c.513C>T	ENSP00000365770.1:p.Cys171=
ENST00000376590.7:c.390C>T	ENSP00000365775.3:p.Cys130=
ENST00000376592.5:c.390C>T	ENSP00000365777.1:p.Cys130=
ENST00000418034.1:c.390C>T	ENSP00000405082.1:p.Cys130=
NM_005957.4:c.390C>T , LRG_726t1:c.390C>T	NP_005948.3:p.Cys130=
XM_005263458.2:c.513C>T	XP_005263515.1:p.Cys171=
XM_005263460.3:c.390C>T	XP_005263517.1:p.Cys130=
XM_005263461.3:c.390C>T	XP_005263518.1:p.Cys130=
XM_005263462.3:c.390C>T	XP_005263519.1:p.Cys130=
XM_005263463.2:c.144C>T	XP_005263520.1:p.Cys48=
XM_011541495.1:c.510C>T	XP_011539797.1:p.Cys170=
XM_011541496.1:c.513C>T	XP_011539798.1:p.Cys171=
NM_001330358.1:c.513C>T	NP_001317287.1:p.Cys171=
XM_005263460.5:c.390C>T	XP_005263517.1:p.Cys130=
XM_005263462.4:c.390C>T	XP_005263519.1:p.Cys130=
XM_005263463.4:c.144C>T	XP_005263520.1:p.Cys48=
XM_011541495.3:c.510C>T	XP_011539797.1:p.Cys170=
XM_011541496.3:c.513C>T	XP_011539798.1:p.Cys171=
XM_017001328.2:c.513C>T	XP_016856817.1:p.Cys171=
XM_024447198.1:c.144C>T	XP_024302966.1:p.Cys48=
XR_002956640.1:n.1257C>T
NM_005957.5:c.390C>T MANE Select	NP_005948.3:p.Cys130=
NM_001330358.2:c.513C>T	NP_001317287.1:p.Cys171=