Canonical Allele Identifier: CA2686114346
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs2117225317
gnomAD v4: 8-10622557-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622557A>C , CM000670.2:g.10622557A>C GRCh38
NC_000008.10:g.10480067A>C , CM000670.1:g.10480067A>C GRCh37
NC_000008.9:g.10517477A>C NCBI36
NG_028035.1:g.37551T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.609+36T>G MANE Select ENSP00000371923.3:n.609+36T>G
ENST00000329335.3:n.859+36T>G
ENST00000382483.3:c.609+36T>G ENSP00000371923.3:n.609+36T>G
NM_178857.5:c.609+36T>G NP_849188.4:n.609+36T>G
NM_178857.6:c.609+36T>G MANE Select NP_849188.4:n.609+36T>G