Canonical Allele Identifier: CA1260705287
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs1670624061
gnomAD v4: 2-72891616-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891616G>C , CM000664.2:g.72891616G>C GRCh38
NC_000002.11:g.73118745G>C , CM000664.1:g.73118745G>C GRCh37
NC_000002.10:g.72972253G>C NCBI36
NG_008234.1:g.9234G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*79G>C MANE Select ENSP00000234454.5:n.*79G>C
ENST00000234454.5:c.*79G>C ENSP00000234454.5:n.*79G>C
ENST00000498749.1:n.810G>C
NM_003124.4:c.*79G>C NP_003115.1:n.*79G>C
NM_003124.5:c.*79G>C MANE Select NP_003115.1:n.*79G>C
Search 100 bp 5'
Search 100 bp 3'