Canonical Allele Identifier: CA49798903
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs971120060
gnomAD v4: 2-72891715-A-G
MyVariant Identifiers: chr2:g.73118844A>G (hg19) chr2:g.72891715A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891715A>G , CM000664.2:g.72891715A>G GRCh38
NC_000002.11:g.73118844A>G , CM000664.1:g.73118844A>G GRCh37
NC_000002.10:g.72972352A>G NCBI36
NG_008234.1:g.9333A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*178A>G MANE Select ENSP00000234454.5:n.*178A>G
ENST00000234454.5:c.*178A>G ENSP00000234454.5:n.*178A>G
ENST00000498749.1:n.909A>G
NM_003124.4:c.*178A>G NP_003115.1:n.*178A>G
NM_003124.5:c.*178A>G MANE Select NP_003115.1:n.*178A>G
Search 100 bp 5'
Search 100 bp 3'