Canonical Allele Identifier: CA370295542
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1218261304
gnomAD v2: 8-10470186-C-A
gnomAD v4: 8-10612676-C-A
MyVariant Identifiers: chr8:g.10470186C>A (hg19) chr8:g.10612676C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612676C>A , CM000670.2:g.10612676C>A GRCh38
NC_000008.10:g.10470186C>A , CM000670.1:g.10470186C>A GRCh37
NC_000008.9:g.10507596C>A NCBI36
NG_028035.1:g.47432G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.1422G>T MANE Select ENSP00000371923.3:p.Arg474Ser
ENST00000382483.3:c.1422G>T ENSP00000371923.3:p.Arg474Ser
NM_178857.5:c.1422G>T NP_849188.4:p.Arg474Ser
NM_178857.6:c.1422G>T MANE Select NP_849188.4:p.Arg474Ser
Search 100 bp 5'
Search 100 bp 3'