Canonical Allele Identifier: CA2659569788
Gene: SPR HGNC NCBI

Linked Data

gnomAD v4: 2-72891618-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891618C>T , CM000664.2:g.72891618C>T GRCh38
NC_000002.11:g.73118747C>T , CM000664.1:g.73118747C>T GRCh37
NC_000002.10:g.72972255C>T NCBI36
NG_008234.1:g.9236C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*81C>T MANE Select ENSP00000234454.5:n.*81C>T
ENST00000234454.5:c.*81C>T ENSP00000234454.5:n.*81C>T
ENST00000498749.1:n.812C>T
NM_003124.4:c.*81C>T NP_003115.1:n.*81C>T
NM_003124.5:c.*81C>T MANE Select NP_003115.1:n.*81C>T
Search 100 bp 5'
Search 100 bp 3'