LDH info

Canonical Allele Identifier: CA16077532
Gene: CR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3818361

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207611623A>G , CM000663.2:g.207611623A>G GRCh38
NC_000001.10:g.207784968A>G , CM000663.1:g.207784968A>G GRCh37
NC_000001.9:g.205851591A>G NCBI36
NG_007481.1:g.120496A>G

Transcript Alleles

HGVS Amino-acid change
NM_000573.3:c.4946-54A>G VV NP_000564.2:p.=
NM_000651.4:c.6296-54A>G VV NP_000642.3:p.=
XM_006711166.2:c.6311-54A>G XP_006711229.1:p.=
XM_011509205.1:c.6311-54A>G XP_011507507.1:p.=
NM_000651.5:c.6296-54A>G VV NP_000642.3:p.=
XM_024453287.1:c.4961-54A>G XP_024309055.1:p.=
NM_000573.4:c.4946-54A>G VV NP_000564.2:p.=
NM_000651.6:c.6296-54A>G VV NP_000642.3:p.=
ENST00000367049.8:n.6296-54A>G ENSP00000356016.4:p.=
ENST00000367051.5:c.4946-54A>G ENSP00000356018.1:p.=
ENST00000367052.5:c.4946-54A>G ENSP00000356019.1:p.=
ENST00000367053.5:c.4946-54A>G ENSP00000356020.1:p.=
ENST00000400960.6:c.4946-54A>G ENSP00000383744.2:p.=
ENST00000529814.1:n.1180-4952A>G