Canonical Allele Identifier: CA426703453
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118477T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891348T>A , CM000664.2:g.72891348T>A GRCh38
NC_000002.11:g.73118477T>A , CM000664.1:g.73118477T>A GRCh37
NC_000002.10:g.72971985T>A NCBI36
NG_008234.1:g.8966T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.597T>A MANE Select ENSP00000234454.5:p.Gly199=
ENST00000234454.5:c.597T>A ENSP00000234454.5:p.Gly199=
ENST00000498749.1:n.542T>A
NM_003124.4:c.597T>A NP_003115.1:p.Gly199=
NM_003124.5:c.597T>A MANE Select NP_003115.1:p.Gly199=
Search 100 bp 5'
Search 100 bp 3'