Canonical Allele Identifier: CA1014681035
Gene: SLC52A3 HGNC NCBI

Linked Data

dbSNP Id: rs1986670459
gnomAD v3: 20-765859-G-C
gnomAD v4: 20-765859-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.765859G>C , CM000682.2:g.765859G>C GRCh38
NC_000020.10:g.746503G>C , CM000682.1:g.746503G>C GRCh37
NC_000020.9:g.694503G>C NCBI36
NG_027687.1:g.7726C>G
NG_027687.2:g.15127C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381944.5:c.-51-34C>G ENSP00000371370.3:n.-51-34C>G
ENST00000488495.3:c.-85C>G ENSP00000494009.1:n.-85C>G
ENST00000645534.1:c.-51-34C>G MANE Select ENSP00000494193.1:n.-51-34C>G
ENST00000674666.1:c.-85C>G ENSP00000502783.1:n.-85C>G
ENST00000675066.1:c.-51-34C>G ENSP00000501902.1:n.-51-34C>G
ENST00000676154.1:c.-51-34C>G ENSP00000501807.1:n.-51-34C>G
ENST00000217254.11:c.-51-34C>G ENSP00000217254.7:n.-51-34C>G
ENST00000381944.4:c.-51-34C>G ENSP00000371370.3:n.-51-34C>G
ENST00000632431.1:c.-51-34C>G ENSP00000488723.1:n.-51-34C>G
NM_033409.3:c.-51-34C>G NP_212134.3:n.-51-34C>G
XM_005260655.3:c.-51-34C>G XP_005260712.1:n.-51-34C>G
XM_011529148.1:c.-85C>G XP_011527450.1:n.-85C>G
XM_005260655.4:c.-51-34C>G XP_005260712.1:n.-51-34C>G
XM_024451821.1:c.-51-34C>G XP_024307589.1:n.-51-34C>G
NM_033409.4:c.-51-34C>G MANE Select NP_212134.3:n.-51-34C>G
NM_001370085.1:c.-51-34C>G NP_001357014.1:n.-51-34C>G
NM_001370086.1:c.-85C>G NP_001357015.1:n.-85C>G