Canonical Allele Identifier: CA2617917091

Gene: LDHB

Linked Data

• gnomAD v4: 12-21641939-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21641939T>G , CM000674.2:g.21641939T>G	GRCh38
NC_000012.11:g.21794873T>G , CM000674.1:g.21794873T>G	GRCh37
NC_000012.10:g.21686140T>G	NCBI36
NG_017038.1:g.20917A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647960.1:c.595+13A>C	ENSP00000497202.1:n.595+13A>C
ENST00000673047.2:c.595+13A>C	ENSP00000500484.2:n.595+13A>C
ENST00000350669.5:c.595+13A>C MANE Select	ENSP00000229319.1:n.595+13A>C
ENST00000396075.5:c.595+13A>C	ENSP00000379385.1:n.595+13A>C
ENST00000396076.5:c.595+13A>C	ENSP00000379386.1:n.595+13A>C
NM_001174097.1:c.595+13A>C	NP_001167568.1:n.595+13A>C
NM_001174097.2:c.595+13A>C	NP_001167568.1:n.595+13A>C
NM_001315537.1:c.595+13A>C	NP_001302466.1:n.595+13A>C
NM_002300.6:c.595+13A>C	NP_002291.1:n.595+13A>C
NM_002300.7:c.595+13A>C	NP_002291.1:n.595+13A>C
XM_006719074.2:c.595+13A>C	XP_006719137.1:n.595+13A>C
NM_001174097.3:c.595+13A>C	NP_001167568.1:n.595+13A>C
NM_001315537.2:c.595+13A>C	NP_001302466.1:n.595+13A>C
NM_002300.8:c.595+13A>C MANE Select	NP_002291.1:n.595+13A>C