Canonical Allele Identifier: CA370295463
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs978884122
gnomAD v2: 8-10470146-G-A
gnomAD v4: 8-10612636-G-A
COSMIC: COSM3924417
MyVariant Identifiers: chr8:g.10470146G>A (hg19) chr8:g.10612636G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612636G>A , CM000670.2:g.10612636G>A GRCh38
NC_000008.10:g.10470146G>A , CM000670.1:g.10470146G>A GRCh37
NC_000008.9:g.10507556G>A NCBI36
NG_028035.1:g.47472C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1462C>T MANE Select ENSP00000371923.3:p.Gln488Ter
ENST00000382483.3:c.1462C>T ENSP00000371923.3:p.Gln488Ter
NM_178857.5:c.1462C>T NP_849188.4:p.Gln488Ter
NM_178857.6:c.1462C>T MANE Select NP_849188.4:p.Gln488Ter
Search 100 bp 5'
Search 100 bp 3'