Canonical Allele Identifier: CA347232916
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118654C>G (hg19) chr2:g.72891525C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891525C>G , CM000664.2:g.72891525C>G GRCh38
NC_000002.11:g.73118654C>G , CM000664.1:g.73118654C>G GRCh37
NC_000002.10:g.72972162C>G NCBI36
NG_008234.1:g.9143C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.774C>G MANE Select ENSP00000234454.5:p.Phe258Leu
ENST00000234454.5:c.774C>G ENSP00000234454.5:p.Phe258Leu
ENST00000498749.1:n.719C>G
NM_003124.4:c.774C>G NP_003115.1:p.Phe258Leu
NM_003124.5:c.774C>G MANE Select NP_003115.1:p.Phe258Leu
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