Canonical Allele Identifier: CA2659569768
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891574-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891574A>C , CM000664.2:g.72891574A>C GRCh38
NC_000002.11:g.73118703A>C , CM000664.1:g.73118703A>C GRCh37
NC_000002.10:g.72972211A>C NCBI36
NG_008234.1:g.9192A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*37A>C MANE Select ENSP00000234454.5:n.*37A>C
ENST00000234454.5:c.*37A>C ENSP00000234454.5:n.*37A>C
ENST00000498749.1:n.768A>C
NM_003124.4:c.*37A>C NP_003115.1:n.*37A>C
NM_003124.5:c.*37A>C MANE Select NP_003115.1:n.*37A>C
Search 100 bp 5'
Search 100 bp 3'