Canonical Allele Identifier: CA347232393
Gene: SPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.73118495G>A (hg19) chr2:g.72891366G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891366G>A , CM000664.2:g.72891366G>A GRCh38
NC_000002.11:g.73118495G>A , CM000664.1:g.73118495G>A GRCh37
NC_000002.10:g.72972003G>A NCBI36
NG_008234.1:g.8984G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.615G>A MANE Select ENSP00000234454.5:p.Met205Ile
ENST00000234454.5:c.615G>A ENSP00000234454.5:p.Met205Ile
ENST00000498749.1:n.560G>A
NM_003124.4:c.615G>A NP_003115.1:p.Met205Ile
NM_003124.5:c.615G>A MANE Select NP_003115.1:p.Met205Ile
Search 100 bp 5'
Search 100 bp 3'