Canonical Allele Identifier: CA413658055
Gene: SLC16A2 HGNC NCBI

Linked Data

dbSNP Id: rs1422998437
gnomAD v2: X-73745689-C-G
gnomAD v4: X-74525854-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525854C>G , CM000685.2:g.74525854C>G GRCh38
NC_000023.10:g.73745689C>G , CM000685.1:g.73745689C>G GRCh37
NC_000023.9:g.73662414C>G NCBI36
NG_011641.1:g.109605C>G
NG_011641.2:g.109605C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1131C>G MANE Select ENSP00000465734.1:p.Ile377Met
ENST00000636771.1:c.1040C>G
ENST00000587091.5:c.1131C>G ENSP00000465734.1:p.Ile377Met
ENST00000590447.1:c.571C>G
NM_006517.4:c.1131C>G NP_006508.2:p.Ile377Met
XM_005262294.1:c.1131C>G XP_005262351.1:p.Ile377Met
NM_006517.5:c.1131C>G MANE Select NP_006508.2:p.Ile377Met