Canonical Allele Identifier: CA372385774
Gene: SLURP1 HGNC NCBI

Linked Data

dbSNP Id: rs121908317
gnomAD v2: 8-143822587-G-C
gnomAD v4: 8-142741169-G-C
MyVariant Identifiers: chr8:g.143822587G>C (hg19) chr8:g.142741169G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142741169G>C , CM000670.2:g.142741169G>C GRCh38
NC_000008.10:g.143822587G>C , CM000670.1:g.143822587G>C GRCh37
NC_000008.9:g.143819589G>C NCBI36
NG_011494.1:g.6243C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000246515.2:c.286C>G MANE Select ENSP00000246515.1:p.Arg96Gly
ENST00000246515.1:c.286C>G ENSP00000246515.1:p.Arg96Gly
NM_020427.2:c.286C>G NP_065160.1:p.Arg96Gly
NM_020427.3:c.286C>G MANE Select NP_065160.1:p.Arg96Gly
Search 100 bp 5'
Search 100 bp 3'