LDH info

Canonical Allele Identifier: CA15724860
Gene: ACVR1B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12809597

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51962539T>G , CM000674.2:g.51962539T>G GRCh38
NC_000012.11:g.52356323T>G , CM000674.1:g.52356323T>G GRCh37
NC_000012.10:g.50642590T>G NCBI36
NG_022926.1:g.15873T>G

Transcript Alleles

HGVS Amino-acid change
NM_004302.4:c.91+10705T>G VV NP_004293.1:p.=
NM_020327.3:c.-66+9040T>G VV NP_064732.3:p.=
NM_020328.3:c.91+10705T>G VV NP_064733.3:p.=
XM_011538966.1:c.91+10705T>G XP_011537268.1:p.=
XM_011538967.1:c.91+10705T>G XP_011537269.1:p.=
XM_011538966.3:c.91+10705T>G XP_011537268.1:p.=
XM_011538967.3:c.91+10705T>G XP_011537269.1:p.=
XM_017020201.2:c.91+10705T>G XP_016875690.1:p.=
NM_004302.5:c.91+10705T>G VV MANE Preferred NP_004293.1:p.=
NM_020328.4:c.91+10705T>G VV NP_064733.3:p.=
ENST00000257963.8:c.91+10705T>G ENSP00000257963.4:p.=
ENST00000415850.6:n.91+10705T>G ENSP00000397550.2:p.=
ENST00000426655.6:c.91+10705T>G ENSP00000390477.2:p.=
ENST00000536420.5:c.-66+2352T>G ENSP00000443218.1:p.=
ENST00000541224.5:c.91+10705T>G ENSP00000442656.1:p.=
ENST00000542485.1:c.-66+9040T>G ENSP00000442885.1:p.=