Canonical Allele Identifier: CA459619908
Gene: RP1L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.10470063T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612553T>C , CM000670.2:g.10612553T>C GRCh38
NC_000008.10:g.10470063T>C , CM000670.1:g.10470063T>C GRCh37
NC_000008.9:g.10507473T>C NCBI36
NG_028035.1:g.47555A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1545A>G MANE Select ENSP00000371923.3:p.Pro515=
ENST00000382483.3:c.1545A>G ENSP00000371923.3:p.Pro515=
NM_178857.5:c.1545A>G NP_849188.4:p.Pro515=
NM_178857.6:c.1545A>G MANE Select NP_849188.4:p.Pro515=
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Search 100 bp 3'