Canonical Allele Identifier: CA347232830
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118617A>C (hg19) chr2:g.72891488A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891488A>C , CM000664.2:g.72891488A>C GRCh38
NC_000002.11:g.73118617A>C , CM000664.1:g.73118617A>C GRCh37
NC_000002.10:g.72972125A>C NCBI36
NG_008234.1:g.9106A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.737A>C MANE Select ENSP00000234454.5:p.Glu246Ala
ENST00000234454.5:c.737A>C ENSP00000234454.5:p.Glu246Ala
ENST00000498749.1:n.682A>C
NM_003124.4:c.737A>C NP_003115.1:p.Glu246Ala
NM_003124.5:c.737A>C MANE Select NP_003115.1:p.Glu246Ala
Search 100 bp 5'
Search 100 bp 3'