Canonical Allele Identifier: CA892793365
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs1270463787
MyVariant Identifiers: chr2:g.73118785G>T (hg19) chr2:g.72891656G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891656G>T , CM000664.2:g.72891656G>T GRCh38
NC_000002.11:g.73118785G>T , CM000664.1:g.73118785G>T GRCh37
NC_000002.10:g.72972293G>T NCBI36
NG_008234.1:g.9274G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*119G>T MANE Select ENSP00000234454.5:n.*119G>T
ENST00000234454.5:c.*119G>T ENSP00000234454.5:n.*119G>T
ENST00000498749.1:n.850G>T
NM_003124.4:c.*119G>T NP_003115.1:n.*119G>T
NM_003124.5:c.*119G>T MANE Select NP_003115.1:n.*119G>T
Search 100 bp 5'
Search 100 bp 3'