Canonical Allele Identifier: CA886038629

Gene: MTHFR

Linked Data

• dbSNP Id: rs1254659143
• gnomAD v3: 1-11790257-A-G
• gnomAD v4: 1-11790257-A-G
• MyVariant Identifiers: chr1:g.11850314A>G (hg19) ; chr1:g.11790257A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790257A>G , CM000663.2:g.11790257A>G	GRCh38
NC_000001.10:g.11850314A>G , CM000663.1:g.11850314A>G	GRCh37
NC_000001.9:g.11772901A>G	NCBI36
NG_013351.1:g.20847T>C , LRG_726:g.20847T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.*423T>C	ENSP00000365770.1:n.*423T>C
ENST00000376590.9:c.*423T>C MANE Select	ENSP00000365775.3:n.*423T>C
ENST00000376592.6:c.*423T>C	ENSP00000365777.1:n.*423T>C
ENST00000423400.7:c.*423T>C	ENSP00000398908.3:n.*423T>C
ENST00000641446.1:c.*853T>C	ENSP00000493262.1:n.*853T>C
ENST00000641747.1:c.*1906T>C	ENSP00000493116.1:n.*1906T>C
ENST00000641805.1:n.2729T>C
ENST00000376583.7:c.2517T>C	ENSP00000365767.3:n.2517T>C
ENST00000376585.5:c.*423T>C	ENSP00000365770.1:n.*423T>C
ENST00000376590.7:c.*423T>C	ENSP00000365775.3:n.*423T>C
ENST00000376592.5:c.*423T>C	ENSP00000365777.1:n.*423T>C
NM_005957.4:c.*423T>C , LRG_726t1:c.*423T>C	NP_005948.3:n.*423T>C
XM_005263458.2:c.*423T>C	XP_005263515.1:n.*423T>C
XM_005263460.3:c.*423T>C	XP_005263517.1:n.*423T>C
XM_005263461.3:c.*423T>C	XP_005263518.1:n.*423T>C
XM_005263462.3:c.*423T>C	XP_005263519.1:n.*423T>C
XM_005263463.2:c.*423T>C	XP_005263520.1:n.*423T>C
XM_011541495.1:c.*423T>C	XP_011539797.1:n.*423T>C
XM_011541496.1:c.*283T>C	XP_011539798.1:n.*283T>C
NM_001330358.1:c.*423T>C	NP_001317287.1:n.*423T>C
XM_005263460.5:c.*423T>C	XP_005263517.1:n.*423T>C
XM_005263462.4:c.*423T>C	XP_005263519.1:n.*423T>C
XM_005263463.4:c.*423T>C	XP_005263520.1:n.*423T>C
XM_011541495.3:c.*423T>C	XP_011539797.1:n.*423T>C
XM_011541496.3:c.*283T>C	XP_011539798.1:n.*283T>C
XM_024447198.1:c.*423T>C	XP_024302966.1:n.*423T>C
NM_005957.5:c.*423T>C MANE Select	NP_005948.3:n.*423T>C
NM_001330358.2:c.*423T>C	NP_001317287.1:n.*423T>C