Canonical Allele Identifier: CA2659569758
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891549-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891549T>G , CM000664.2:g.72891549T>G GRCh38
NC_000002.11:g.73118678T>G , CM000664.1:g.73118678T>G GRCh37
NC_000002.10:g.72972186T>G NCBI36
NG_008234.1:g.9167T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*12T>G MANE Select ENSP00000234454.5:n.*12T>G
ENST00000234454.5:c.*12T>G ENSP00000234454.5:n.*12T>G
ENST00000498749.1:n.743T>G
NM_003124.4:c.*12T>G NP_003115.1:n.*12T>G
NM_003124.5:c.*12T>G MANE Select NP_003115.1:n.*12T>G
Search 100 bp 5'
Search 100 bp 3'