Canonical Allele Identifier: CA459617032
Gene: RP1L1 HGNC NCBI

Linked Data

gnomAD v3: 8-10608206-C-T
gnomAD v4: 8-10608206-C-T
MyVariant Identifiers: chr8:g.10465716C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10608206C>T , CM000670.2:g.10608206C>T GRCh38
NC_000008.10:g.10465716C>T , CM000670.1:g.10465716C>T GRCh37
NC_000008.9:g.10503126C>T NCBI36
NG_028035.1:g.51902G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.5892G>A MANE Select ENSP00000371923.3:p.Gln1964=
ENST00000382483.3:c.5892G>A ENSP00000371923.3:p.Gln1964=
NM_178857.5:c.5892G>A NP_849188.4:p.Gln1964=
NM_178857.6:c.5892G>A MANE Select NP_849188.4:p.Gln1964=
Search 100 bp 5'
Search 100 bp 3'