Canonical Allele Identifier: CA1260705270
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs1670623347
gnomAD v4: 2-72891583-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891583C>G , CM000664.2:g.72891583C>G GRCh38
NC_000002.11:g.73118712C>G , CM000664.1:g.73118712C>G GRCh37
NC_000002.10:g.72972220C>G NCBI36
NG_008234.1:g.9201C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*46C>G MANE Select ENSP00000234454.5:n.*46C>G
ENST00000234454.5:c.*46C>G ENSP00000234454.5:n.*46C>G
ENST00000498749.1:n.777C>G
NM_003124.4:c.*46C>G NP_003115.1:n.*46C>G
NM_003124.5:c.*46C>G MANE Select NP_003115.1:n.*46C>G
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