Canonical Allele Identifier: CA10614364
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 336986
ClinVar RCV Id: RCV000392717
dbSNP Id: rs886056286
gnomAD v2: 2-73114522-C-G
gnomAD v3: 2-72887393-C-G
gnomAD v4: 2-72887393-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72887393C>G , CM000664.2:g.72887393C>G GRCh38
NC_000002.11:g.73114522C>G , CM000664.1:g.73114522C>G GRCh37
NC_000002.10:g.72968030C>G NCBI36
NG_008234.1:g.5011C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.5:c.-40C>G ENSP00000234454.5:n.-40C>G
ENST00000498749.1:n.12C>G
NM_003124.4:c.-40C>G NP_003115.1:n.-40C>G