Canonical Allele Identifier: CA370300106
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1463765797
gnomAD v2: 8-10480255-T-A
gnomAD v3: 8-10622745-T-A
gnomAD v4: 8-10622745-T-A
MyVariant Identifiers: chr8:g.10480255T>A (hg19) chr8:g.10622745T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622745T>A , CM000670.2:g.10622745T>A GRCh38
NC_000008.10:g.10480255T>A , CM000670.1:g.10480255T>A GRCh37
NC_000008.9:g.10517665T>A NCBI36
NG_028035.1:g.37363A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.457A>T MANE Select ENSP00000371923.3:p.Arg153Trp
ENST00000329335.3:n.707A>T
ENST00000382483.3:c.457A>T ENSP00000371923.3:p.Arg153Trp
NM_178857.5:c.457A>T NP_849188.4:p.Arg153Trp
NM_178857.6:c.457A>T MANE Select NP_849188.4:p.Arg153Trp
Search 100 bp 5'
Search 100 bp 3'