Canonical Allele Identifier: CA426703549
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118561A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891432A>G , CM000664.2:g.72891432A>G GRCh38
NC_000002.11:g.73118561A>G , CM000664.1:g.73118561A>G GRCh37
NC_000002.10:g.72972069A>G NCBI36
NG_008234.1:g.9050A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.681A>G MANE Select ENSP00000234454.5:p.Ala227=
ENST00000234454.5:c.681A>G ENSP00000234454.5:p.Ala227=
ENST00000498749.1:n.626A>G
NM_003124.4:c.681A>G NP_003115.1:p.Ala227=
NM_003124.5:c.681A>G MANE Select NP_003115.1:p.Ala227=
Search 100 bp 5'
Search 100 bp 3'