Canonical Allele Identifier: CA347232922
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118657T>A (hg19) chr2:g.72891528T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891528T>A , CM000664.2:g.72891528T>A GRCh38
NC_000002.11:g.73118657T>A , CM000664.1:g.73118657T>A GRCh37
NC_000002.10:g.72972165T>A NCBI36
NG_008234.1:g.9146T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.777T>A MANE Select ENSP00000234454.5:p.Tyr259Ter
ENST00000234454.5:c.777T>A ENSP00000234454.5:p.Tyr259Ter
ENST00000498749.1:n.722T>A
NM_003124.4:c.777T>A NP_003115.1:p.Tyr259Ter
NM_003124.5:c.777T>A MANE Select NP_003115.1:p.Tyr259Ter
Search 100 bp 5'
Search 100 bp 3'