Canonical Allele Identifier: CA459619849
Gene: RP1L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.10480109C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622599C>A , CM000670.2:g.10622599C>A GRCh38
NC_000008.10:g.10480109C>A , CM000670.1:g.10480109C>A GRCh37
NC_000008.9:g.10517519C>A NCBI36
NG_028035.1:g.37509G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.603G>T MANE Select ENSP00000371923.3:p.Gly201=
ENST00000329335.3:n.853G>T
ENST00000382483.3:c.603G>T ENSP00000371923.3:p.Gly201=
NM_178857.5:c.603G>T NP_849188.4:p.Gly201=
NM_178857.6:c.603G>T MANE Select NP_849188.4:p.Gly201=
Search 100 bp 5'
Search 100 bp 3'