Canonical Allele Identifier: CA2659569865
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891693-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891693C>G , CM000664.2:g.72891693C>G GRCh38
NC_000002.11:g.73118822C>G , CM000664.1:g.73118822C>G GRCh37
NC_000002.10:g.72972330C>G NCBI36
NG_008234.1:g.9311C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*156C>G MANE Select ENSP00000234454.5:n.*156C>G
ENST00000234454.5:c.*156C>G ENSP00000234454.5:n.*156C>G
ENST00000498749.1:n.887C>G
NM_003124.4:c.*156C>G NP_003115.1:n.*156C>G
NM_003124.5:c.*156C>G MANE Select NP_003115.1:n.*156C>G
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