Canonical Allele Identifier: CA426703708
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118636T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891507T>G , CM000664.2:g.72891507T>G GRCh38
NC_000002.11:g.73118636T>G , CM000664.1:g.73118636T>G GRCh37
NC_000002.10:g.72972144T>G NCBI36
NG_008234.1:g.9125T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.756T>G MANE Select ENSP00000234454.5:p.Ser252=
ENST00000234454.5:c.756T>G ENSP00000234454.5:p.Ser252=
ENST00000498749.1:n.701T>G
NM_003124.4:c.756T>G NP_003115.1:p.Ser252=
NM_003124.5:c.756T>G MANE Select NP_003115.1:p.Ser252=
Search 100 bp 5'
Search 100 bp 3'