Canonical Allele Identifier: CA533656137
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs1345821577
gnomAD v2: 2-73118754-G-A
gnomAD v3: 2-72891625-G-A
gnomAD v4: 2-72891625-G-A
MyVariant Identifiers: chr2:g.73118754G>A (hg19) chr2:g.72891625G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891625G>A , CM000664.2:g.72891625G>A GRCh38
NC_000002.11:g.73118754G>A , CM000664.1:g.73118754G>A GRCh37
NC_000002.10:g.72972262G>A NCBI36
NG_008234.1:g.9243G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*88G>A MANE Select ENSP00000234454.5:n.*88G>A
ENST00000234454.5:c.*88G>A ENSP00000234454.5:n.*88G>A
ENST00000498749.1:n.819G>A
NM_003124.4:c.*88G>A NP_003115.1:n.*88G>A
NM_003124.5:c.*88G>A MANE Select NP_003115.1:n.*88G>A
Search 100 bp 5'
Search 100 bp 3'