Canonical Allele Identifier: CA595464
Gene: MTHFR HGNC NCBI

Linked Data

ClinVar Variation Id: 499432
dbSNP Id: rs2066464
gnomAD v2: 1-11854926-T-C
gnomAD v3: 1-11794869-T-C
gnomAD v4: 1-11794869-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11794869T>C , CM000663.2:g.11794869T>C GRCh38
NC_000001.10:g.11854926T>C , CM000663.1:g.11854926T>C GRCh37
NC_000001.9:g.11777513T>C NCBI36
NG_013351.1:g.16235A>G , LRG_726:g.16235A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376585.6:c.1155-6A>G ENSP00000365770.1:n.1155-6A>G
ENST00000376590.9:c.1032-6A>G MANE Select ENSP00000365775.3:n.1032-6A>G
ENST00000376592.6:c.1032-6A>G ENSP00000365777.1:n.1032-6A>G
ENST00000423400.7:c.1152-6A>G ENSP00000398908.3:n.1152-6A>G
ENST00000641407.1:c.1032-6A>G ENSP00000493098.1:n.1032-6A>G
ENST00000641446.1:c.1032-6A>G ENSP00000493262.1:n.1032-6A>G
ENST00000641747.1:c.*544-6A>G ENSP00000493116.1:n.*544-6A>G
ENST00000641759.1:n.1395A>G
ENST00000641805.1:n.1543A>G
ENST00000641820.1:c.297-6A>G ENSP00000492937.1:n.297-6A>G
ENST00000376583.7:c.1155-6A>G ENSP00000365767.3:n.1155-6A>G
ENST00000376585.5:c.1155-6A>G ENSP00000365770.1:n.1155-6A>G
ENST00000376590.7:c.1032-6A>G ENSP00000365775.3:n.1032-6A>G
ENST00000376592.5:c.1032-6A>G ENSP00000365777.1:n.1032-6A>G
NM_005957.4:c.1032-6A>G , LRG_726t1:c.1032-6A>G NP_005948.3:n.1032-6A>G
XM_005263458.2:c.1155-6A>G XP_005263515.1:n.1155-6A>G
XM_005263460.3:c.1032-6A>G XP_005263517.1:n.1032-6A>G
XM_005263461.3:c.1032-6A>G XP_005263518.1:n.1032-6A>G
XM_005263462.3:c.1032-6A>G XP_005263519.1:n.1032-6A>G
XM_005263463.2:c.786-6A>G XP_005263520.1:n.786-6A>G
XM_011541495.1:c.1152-6A>G XP_011539797.1:n.1152-6A>G
XM_011541496.1:c.1155-6A>G XP_011539798.1:n.1155-6A>G
NM_001330358.1:c.1155-6A>G NP_001317287.1:n.1155-6A>G
XM_005263460.5:c.1032-6A>G XP_005263517.1:n.1032-6A>G
XM_005263462.4:c.1032-6A>G XP_005263519.1:n.1032-6A>G
XM_005263463.4:c.786-6A>G XP_005263520.1:n.786-6A>G
XM_011541495.3:c.1152-6A>G XP_011539797.1:n.1152-6A>G
XM_011541496.3:c.1155-6A>G XP_011539798.1:n.1155-6A>G
XM_017001328.2:c.1155-6A>G XP_016856817.1:n.1155-6A>G
XM_024447198.1:c.786-6A>G XP_024302966.1:n.786-6A>G
XR_002956640.1:n.2127A>G
NM_005957.5:c.1032-6A>G MANE Select NP_005948.3:n.1032-6A>G
NM_001330358.2:c.1155-6A>G NP_001317287.1:n.1155-6A>G