Canonical Allele Identifier: CA892793370
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs1361534807
MyVariant Identifiers: chr2:g.73118792G>A (hg19) chr2:g.72891663G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891663G>A , CM000664.2:g.72891663G>A GRCh38
NC_000002.11:g.73118792G>A , CM000664.1:g.73118792G>A GRCh37
NC_000002.10:g.72972300G>A NCBI36
NG_008234.1:g.9281G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*126G>A MANE Select ENSP00000234454.5:n.*126G>A
ENST00000234454.5:c.*126G>A ENSP00000234454.5:n.*126G>A
ENST00000498749.1:n.857G>A
NM_003124.4:c.*126G>A NP_003115.1:n.*126G>A
NM_003124.5:c.*126G>A MANE Select NP_003115.1:n.*126G>A
Search 100 bp 5'
Search 100 bp 3'