Canonical Allele Identifier: CA2659569777
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891598-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891598T>C , CM000664.2:g.72891598T>C GRCh38
NC_000002.11:g.73118727T>C , CM000664.1:g.73118727T>C GRCh37
NC_000002.10:g.72972235T>C NCBI36
NG_008234.1:g.9216T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*61T>C MANE Select ENSP00000234454.5:n.*61T>C
ENST00000234454.5:c.*61T>C ENSP00000234454.5:n.*61T>C
ENST00000498749.1:n.792T>C
NM_003124.4:c.*61T>C NP_003115.1:n.*61T>C
NM_003124.5:c.*61T>C MANE Select NP_003115.1:n.*61T>C
Search 100 bp 5'
Search 100 bp 3'