Canonical Allele Identifier: CA17998713

Gene: MTHFR

Linked Data

• dbSNP Id: rs569658202
• gnomAD v3: 1-11790238-A-C
• gnomAD v4: 1-11790238-A-C
• MyVariant Identifiers: chr1:g.11850295A>C (hg19) ; chr1:g.11790238A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11790238A>C , CM000663.2:g.11790238A>C	GRCh38
NC_000001.10:g.11850295A>C , CM000663.1:g.11850295A>C	GRCh37
NC_000001.9:g.11772882A>C	NCBI36
NG_013351.1:g.20866T>G , LRG_726:g.20866T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376585.6:c.*442T>G	ENSP00000365770.1:n.*442T>G
ENST00000376590.9:c.*442T>G MANE Select	ENSP00000365775.3:n.*442T>G
ENST00000376592.6:c.*442T>G	ENSP00000365777.1:n.*442T>G
ENST00000423400.7:c.*442T>G	ENSP00000398908.3:n.*442T>G
ENST00000641446.1:c.*872T>G	ENSP00000493262.1:n.*872T>G
ENST00000641747.1:c.*1925T>G	ENSP00000493116.1:n.*1925T>G
ENST00000641805.1:n.2748T>G
ENST00000376583.7:c.2536T>G	ENSP00000365767.3:n.2536T>G
ENST00000376585.5:c.*442T>G	ENSP00000365770.1:n.*442T>G
ENST00000376590.7:c.*442T>G	ENSP00000365775.3:n.*442T>G
ENST00000376592.5:c.*442T>G	ENSP00000365777.1:n.*442T>G
NM_005957.4:c.*442T>G , LRG_726t1:c.*442T>G	NP_005948.3:n.*442T>G
XM_005263458.2:c.*442T>G	XP_005263515.1:n.*442T>G
XM_005263460.3:c.*442T>G	XP_005263517.1:n.*442T>G
XM_005263461.3:c.*442T>G	XP_005263518.1:n.*442T>G
XM_005263462.3:c.*442T>G	XP_005263519.1:n.*442T>G
XM_005263463.2:c.*442T>G	XP_005263520.1:n.*442T>G
XM_011541495.1:c.*442T>G	XP_011539797.1:n.*442T>G
XM_011541496.1:c.*302T>G	XP_011539798.1:n.*302T>G
NM_001330358.1:c.*442T>G	NP_001317287.1:n.*442T>G
XM_005263460.5:c.*442T>G	XP_005263517.1:n.*442T>G
XM_005263462.4:c.*442T>G	XP_005263519.1:n.*442T>G
XM_005263463.4:c.*442T>G	XP_005263520.1:n.*442T>G
XM_011541495.3:c.*442T>G	XP_011539797.1:n.*442T>G
XM_011541496.3:c.*302T>G	XP_011539798.1:n.*302T>G
XM_024447198.1:c.*442T>G	XP_024302966.1:n.*442T>G
NM_005957.5:c.*442T>G MANE Select	NP_005948.3:n.*442T>G
NM_001330358.2:c.*442T>G	NP_001317287.1:n.*442T>G