Canonical Allele Identifier: CA998623873

Gene: MTHFR

Linked Data

• dbSNP Id: rs1644393731
• gnomAD v3: 1-11801893-C-T
• gnomAD v4: 1-11801893-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11801893C>T , CM000663.2:g.11801893C>T	GRCh38
NC_000001.10:g.11861950C>T , CM000663.1:g.11861950C>T	GRCh37
NC_000001.9:g.11784537C>T	NCBI36
NG_008766.1:g.744C>T
NG_013351.1:g.9211G>A , LRG_726:g.9211G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376486.3:c.237-494G>A	ENSP00000365669.3:n.237-494G>A
ENST00000376585.6:c.360-494G>A	ENSP00000365770.1:n.360-494G>A
ENST00000376590.9:c.237-494G>A MANE Select	ENSP00000365775.3:n.237-494G>A
ENST00000376592.6:c.237-494G>A	ENSP00000365777.1:n.237-494G>A
ENST00000423400.7:c.357-494G>A	ENSP00000398908.3:n.357-494G>A
ENST00000431243.6:n.1018-477G>A
ENST00000641407.1:c.237-494G>A	ENSP00000493098.1:n.237-494G>A
ENST00000641437.1:n.369-494G>A
ENST00000641446.1:c.237-494G>A	ENSP00000493262.1:n.237-494G>A
ENST00000641721.1:n.294-494G>A
ENST00000641747.1:c.236+988G>A	ENSP00000493116.1:n.236+988G>A
ENST00000641759.1:n.372-494G>A
ENST00000641805.1:n.520-494G>A
ENST00000641909.1:n.647-494G>A
ENST00000642002.1:n.466-477G>A
ENST00000376583.7:c.360-494G>A	ENSP00000365767.3:n.360-494G>A
ENST00000376585.5:c.360-494G>A	ENSP00000365770.1:n.360-494G>A
ENST00000376590.7:c.237-494G>A	ENSP00000365775.3:n.237-494G>A
ENST00000376592.5:c.237-494G>A	ENSP00000365777.1:n.237-494G>A
ENST00000418034.1:c.237-494G>A	ENSP00000405082.1:n.237-494G>A
NM_005957.4:c.237-494G>A , LRG_726t1:c.237-494G>A	NP_005948.3:n.237-494G>A
XM_005263458.2:c.360-494G>A	XP_005263515.1:n.360-494G>A
XM_005263460.3:c.237-494G>A	XP_005263517.1:n.237-494G>A
XM_005263461.3:c.237-494G>A	XP_005263518.1:n.237-494G>A
XM_005263462.3:c.237-494G>A	XP_005263519.1:n.237-494G>A
XM_005263463.2:c.-27-477G>A	XP_005263520.1:n.-27-477G>A
XM_011541495.1:c.357-494G>A	XP_011539797.1:n.357-494G>A
XM_011541496.1:c.360-494G>A	XP_011539798.1:n.360-494G>A
NM_001330358.1:c.360-494G>A	NP_001317287.1:n.360-494G>A
XM_005263460.5:c.237-494G>A	XP_005263517.1:n.237-494G>A
XM_005263462.4:c.237-494G>A	XP_005263519.1:n.237-494G>A
XM_005263463.4:c.-27-477G>A	XP_005263520.1:n.-27-477G>A
XM_011541495.3:c.357-494G>A	XP_011539797.1:n.357-494G>A
XM_011541496.3:c.360-494G>A	XP_011539798.1:n.360-494G>A
XM_017001328.2:c.360-494G>A	XP_016856817.1:n.360-494G>A
XM_024447198.1:c.-27-477G>A	XP_024302966.1:n.-27-477G>A
XR_002956640.1:n.1104-494G>A
NM_005957.5:c.237-494G>A MANE Select	NP_005948.3:n.237-494G>A
NM_001330358.2:c.360-494G>A	NP_001317287.1:n.360-494G>A