Canonical Allele Identifier: CA384301567

Gene: LDHB

Linked Data

• MyVariant Identifiers: chr12:g.21794970A>C (hg19) ; chr12:g.21642036A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21642036A>C , CM000674.2:g.21642036A>C	GRCh38
NC_000012.11:g.21794970A>C , CM000674.1:g.21794970A>C	GRCh37
NC_000012.10:g.21686237A>C	NCBI36
NG_017038.1:g.20820T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647960.1:c.511T>G	ENSP00000497202.1:p.Phe171Val
ENST00000673047.2:c.511T>G	ENSP00000500484.2:p.Phe171Val
ENST00000350669.5:c.511T>G MANE Select	ENSP00000229319.1:p.Phe171Val
ENST00000396075.5:c.511T>G	ENSP00000379385.1:p.Phe171Val
ENST00000396076.5:c.511T>G	ENSP00000379386.1:p.Phe171Val
NM_001174097.1:c.511T>G	NP_001167568.1:p.Phe171Val
NM_001174097.2:c.511T>G	NP_001167568.1:p.Phe171Val
NM_001315537.1:c.511T>G	NP_001302466.1:p.Phe171Val
NM_002300.6:c.511T>G	NP_002291.1:p.Phe171Val
NM_002300.7:c.511T>G	NP_002291.1:p.Phe171Val
XM_006719074.2:c.511T>G	XP_006719137.1:p.Phe171Val
NM_001174097.3:c.511T>G	NP_001167568.1:p.Phe171Val
NM_001315537.2:c.511T>G	NP_001302466.1:p.Phe171Val
NM_002300.8:c.511T>G MANE Select	NP_002291.1:p.Phe171Val