LDH info

Canonical Allele Identifier: CA10715109
Gene: MTHFR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13306553

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11800060A>G , CM000663.2:g.11800060A>G GRCh38
NC_000001.10:g.11860117A>G , CM000663.1:g.11860117A>G GRCh37
NC_000001.9:g.11782704A>G NCBI36
NG_013351.1:g.11044T>C , LRG_726:g.11044T>C

Transcript Alleles

HGVS Amino-acid change
NM_005957.4:c.586+152T>C , LRG_726t1:c.586+152T>C NP_005948.3:p.=
XM_005263458.2:c.709+152T>C XP_005263515.1:p.=
XM_005263460.3:c.586+152T>C XP_005263517.1:p.=
XM_005263461.3:c.586+152T>C XP_005263518.1:p.=
XM_005263462.3:c.586+152T>C XP_005263519.1:p.=
XM_005263463.2:c.340+152T>C XP_005263520.1:p.=
XM_011541495.1:c.706+152T>C XP_011539797.1:p.=
XM_011541496.1:c.709+152T>C XP_011539798.1:p.=
NM_001330358.1:c.709+152T>C VV NP_001317287.1:p.=
XM_005263460.5:c.586+152T>C XP_005263517.1:p.=
XM_005263462.4:c.586+152T>C XP_005263519.1:p.=
XM_005263463.4:c.340+152T>C XP_005263520.1:p.=
XM_011541495.3:c.706+152T>C XP_011539797.1:p.=
XM_011541496.3:c.709+152T>C XP_011539798.1:p.=
XM_017001328.2:c.709+152T>C XP_016856817.1:p.=
XM_024447198.1:c.340+152T>C XP_024302966.1:p.=
XR_002956640.1:n.1453+152T>C
ENST00000376583.7:n.709+152T>C ENSP00000365767.3:p.=
ENST00000376585.5:c.709+152T>C ENSP00000365770.1:p.=
ENST00000376590.7:c.586+152T>C ENSP00000365775.3:p.=
ENST00000376592.5:c.586+152T>C ENSP00000365777.1:p.=