Canonical Allele Identifier: CA370295338
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1797885247
gnomAD v4: 8-10612570-C-T
MyVariant Identifiers: chr8:g.10470080C>T (hg19) chr8:g.10612570C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612570C>T , CM000670.2:g.10612570C>T GRCh38
NC_000008.10:g.10470080C>T , CM000670.1:g.10470080C>T GRCh37
NC_000008.9:g.10507490C>T NCBI36
NG_028035.1:g.47538G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.1528G>A MANE Select ENSP00000371923.3:p.Ala510Thr
ENST00000382483.3:c.1528G>A ENSP00000371923.3:p.Ala510Thr
NM_178857.5:c.1528G>A NP_849188.4:p.Ala510Thr
NM_178857.6:c.1528G>A MANE Select NP_849188.4:p.Ala510Thr
Search 100 bp 5'
Search 100 bp 3'