Canonical Allele Identifier: CA171954719
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs773850969
gnomAD v2: 8-10480304-A-G
gnomAD v4: 8-10622794-A-G
MyVariant Identifiers: chr8:g.10480304A>G (hg19) chr8:g.10622794A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622794A>G , CM000670.2:g.10622794A>G GRCh38
NC_000008.10:g.10480304A>G , CM000670.1:g.10480304A>G GRCh37
NC_000008.9:g.10517714A>G NCBI36
NG_028035.1:g.37314T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.408T>C MANE Select ENSP00000371923.3:p.Arg136=
ENST00000329335.3:n.658T>C
ENST00000382483.3:c.408T>C ENSP00000371923.3:p.Arg136=
NM_178857.5:c.408T>C NP_849188.4:p.Arg136=
NM_178857.6:c.408T>C MANE Select NP_849188.4:p.Arg136=
Search 100 bp 5'
Search 100 bp 3'