Canonical Allele Identifier: CA4778924
Gene: LACTB2 HGNC NCBI
LACTB2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3117327
ClinVar RCV Id: RCV004407159
dbSNP Id: rs777106069
gnomAD v2: 8-71574045-G-C
gnomAD v3: 8-70661810-G-C
gnomAD v4: 8-70661810-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.70661810G>C , CM000670.2:g.70661810G>C GRCh38
NC_000008.10:g.71574045G>C , CM000670.1:g.71574045G>C GRCh37
NC_000008.9:g.71736599G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000276590.5:c.210C>G (LACTB2) MANE Select ENSP00000276590.4:p.Ile70Met
ENST00000276590.4:c.210C>G (LACTB2) ENSP00000276590.4:p.Ile70Met
ENST00000522447.5:c.210C>G (LACTB2) ENSP00000428801.1:p.Ile70Met
NM_016027.2:c.210C>G (LACTB2) NP_057111.1:p.Ile70Met
NR_038881.1:n.2247G>C (LACTB2-AS1)
NM_016027.3:c.210C>G (LACTB2) MANE Select NP_057111.1:p.Ile70Met