Canonical Allele Identifier: CA1032174004
Gene: SPR HGNC NCBI

Linked Data

dbSNP Id: rs1670622501
gnomAD v3: 2-72891538-G-T
gnomAD v4: 2-72891538-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.72891538G>T , CM000664.2:g.72891538G>T GRCh38
NC_000002.11:g.73118667G>T , CM000664.1:g.73118667G>T GRCh37
NC_000002.10:g.72972175G>T NCBI36
NG_008234.1:g.9156G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234454.6:c.*1G>T MANE Select ENSP00000234454.5:n.*1G>T
ENST00000234454.5:c.*1G>T ENSP00000234454.5:n.*1G>T
ENST00000498749.1:n.732G>T
NM_003124.4:c.*1G>T NP_003115.1:n.*1G>T
NM_003124.5:c.*1G>T MANE Select NP_003115.1:n.*1G>T
Search 100 bp 5'
Search 100 bp 3'