Canonical Allele Identifier: CA370295901

Gene: RP1L1

Linked Data

• dbSNP Id: rs1797893482
• gnomAD v3: 8-10612859-A-C
• gnomAD v4: 8-10612859-A-C
• MyVariant Identifiers: chr8:g.10470369A>C (hg19) ; chr8:g.10612859A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10612859A>C , CM000670.2:g.10612859A>C	GRCh38
NC_000008.10:g.10470369A>C , CM000670.1:g.10470369A>C	GRCh37
NC_000008.9:g.10507779A>C	NCBI36
NG_028035.1:g.47249T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382483.4:c.1239T>G MANE Select	ENSP00000371923.3:p.His413Gln
ENST00000382483.3:c.1239T>G	ENSP00000371923.3:p.His413Gln
NM_178857.5:c.1239T>G	NP_849188.4:p.His413Gln
NM_178857.6:c.1239T>G MANE Select	NP_849188.4:p.His413Gln