Canonical Allele Identifier: CA347232938
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118664T>C (hg19) chr2:g.72891535T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891535T>C , CM000664.2:g.72891535T>C GRCh38
NC_000002.11:g.73118664T>C , CM000664.1:g.73118664T>C GRCh37
NC_000002.10:g.72972172T>C NCBI36
NG_008234.1:g.9153T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.784T>C MANE Select ENSP00000234454.5:p.Ter262Gln
ENST00000234454.5:c.784T>C ENSP00000234454.5:p.Ter262Gln
ENST00000498749.1:n.729T>C
NM_003124.4:c.784T>C NP_003115.1:p.Ter262Gln
NM_003124.5:c.784T>C MANE Select NP_003115.1:p.Ter262Gln
Search 100 bp 5'
Search 100 bp 3'