Canonical Allele Identifier: CA370299978
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs775422104
gnomAD v3: 8-10622702-G-A
gnomAD v4: 8-10622702-G-A
MyVariant Identifiers: chr8:g.10480212G>A (hg19) chr8:g.10622702G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622702G>A , CM000670.2:g.10622702G>A GRCh38
NC_000008.10:g.10480212G>A , CM000670.1:g.10480212G>A GRCh37
NC_000008.9:g.10517622G>A NCBI36
NG_028035.1:g.37406C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.500C>T MANE Select ENSP00000371923.3:p.Thr167Ile
ENST00000329335.3:n.750C>T
ENST00000382483.3:c.500C>T ENSP00000371923.3:p.Thr167Ile
NM_178857.5:c.500C>T NP_849188.4:p.Thr167Ile
NM_178857.6:c.500C>T MANE Select NP_849188.4:p.Thr167Ile
Search 100 bp 5'
Search 100 bp 3'