Canonical Allele Identifier: CA459620017
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1797892777
gnomAD v4: 8-10612841-T-C
MyVariant Identifiers: chr8:g.10470351T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612841T>C , CM000670.2:g.10612841T>C GRCh38
NC_000008.10:g.10470351T>C , CM000670.1:g.10470351T>C GRCh37
NC_000008.9:g.10507761T>C NCBI36
NG_028035.1:g.47267A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1257A>G MANE Select ENSP00000371923.3:p.Arg419=
ENST00000382483.3:c.1257A>G ENSP00000371923.3:p.Arg419=
NM_178857.5:c.1257A>G NP_849188.4:p.Arg419=
NM_178857.6:c.1257A>G MANE Select NP_849188.4:p.Arg419=
Search 100 bp 5'
Search 100 bp 3'