Canonical Allele Identifier: CA370295887
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1422965511
gnomAD v2: 8-10470362-G-A
gnomAD v4: 8-10612852-G-A
MyVariant Identifiers: chr8:g.10470362G>A (hg19) chr8:g.10612852G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612852G>A , CM000670.2:g.10612852G>A GRCh38
NC_000008.10:g.10470362G>A , CM000670.1:g.10470362G>A GRCh37
NC_000008.9:g.10507772G>A NCBI36
NG_028035.1:g.47256C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.1246C>T MANE Select ENSP00000371923.3:p.Gln416Ter
ENST00000382483.3:c.1246C>T ENSP00000371923.3:p.Gln416Ter
NM_178857.5:c.1246C>T NP_849188.4:p.Gln416Ter
NM_178857.6:c.1246C>T MANE Select NP_849188.4:p.Gln416Ter
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