Canonical Allele Identifier: CA4625110
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs776851437
ExAC: 8:10470000 T / C
gnomAD v2: 8-10470000-T-C
gnomAD v4: 8-10612490-T-C
MyVariant Identifiers: chr8:g.10470000T>C (hg19) chr8:g.10612490T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612490T>C , CM000670.2:g.10612490T>C GRCh38
NC_000008.10:g.10470000T>C , CM000670.1:g.10470000T>C GRCh37
NC_000008.9:g.10507410T>C NCBI36
NG_028035.1:g.47618A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1608A>G MANE Select ENSP00000371923.3:p.Ser536=
ENST00000382483.3:c.1608A>G ENSP00000371923.3:p.Ser536=
NM_178857.5:c.1608A>G NP_849188.4:p.Ser536=
NM_178857.6:c.1608A>G MANE Select NP_849188.4:p.Ser536=
Search 100 bp 5'
Search 100 bp 3'