Canonical Allele Identifier: CA370295347
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1370542929
gnomAD v2: 8-10470085-T-C
gnomAD v3: 8-10612575-T-C
gnomAD v4: 8-10612575-T-C
MyVariant Identifiers: chr8:g.10470085T>C (hg19) chr8:g.10612575T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612575T>C , CM000670.2:g.10612575T>C GRCh38
NC_000008.10:g.10470085T>C , CM000670.1:g.10470085T>C GRCh37
NC_000008.9:g.10507495T>C NCBI36
NG_028035.1:g.47533A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1523A>G MANE Select ENSP00000371923.3:p.Asp508Gly
ENST00000382483.3:c.1523A>G ENSP00000371923.3:p.Asp508Gly
NM_178857.5:c.1523A>G NP_849188.4:p.Asp508Gly
NM_178857.6:c.1523A>G MANE Select NP_849188.4:p.Asp508Gly
Search 100 bp 5'
Search 100 bp 3'