Canonical Allele Identifier: CA2659569772
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891589-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891589C>T , CM000664.2:g.72891589C>T GRCh38
NC_000002.11:g.73118718C>T , CM000664.1:g.73118718C>T GRCh37
NC_000002.10:g.72972226C>T NCBI36
NG_008234.1:g.9207C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*52C>T MANE Select ENSP00000234454.5:n.*52C>T
ENST00000234454.5:c.*52C>T ENSP00000234454.5:n.*52C>T
ENST00000498749.1:n.783C>T
NM_003124.4:c.*52C>T NP_003115.1:n.*52C>T
NM_003124.5:c.*52C>T MANE Select NP_003115.1:n.*52C>T
Search 100 bp 5'
Search 100 bp 3'