Canonical Allele Identifier: CA2659569775
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891593-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891593A>G , CM000664.2:g.72891593A>G GRCh38
NC_000002.11:g.73118722A>G , CM000664.1:g.73118722A>G GRCh37
NC_000002.10:g.72972230A>G NCBI36
NG_008234.1:g.9211A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*56A>G MANE Select ENSP00000234454.5:n.*56A>G
ENST00000234454.5:c.*56A>G ENSP00000234454.5:n.*56A>G
ENST00000498749.1:n.787A>G
NM_003124.4:c.*56A>G NP_003115.1:n.*56A>G
NM_003124.5:c.*56A>G MANE Select NP_003115.1:n.*56A>G
Search 100 bp 5'
Search 100 bp 3'