Canonical Allele Identifier: CA171954494
Gene: RP1L1 HGNC NCBI

Linked Data

dbSNP Id: rs910299586
gnomAD v2: 8-10479928-A-C
gnomAD v3: 8-10622418-A-C
gnomAD v4: 8-10622418-A-C
MyVariant Identifiers: chr8:g.10479928A>C (hg19) chr8:g.10622418A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622418A>C , CM000670.2:g.10622418A>C GRCh38
NC_000008.10:g.10479928A>C , CM000670.1:g.10479928A>C GRCh37
NC_000008.9:g.10517338A>C NCBI36
NG_028035.1:g.37690T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.609+175T>G MANE Select ENSP00000371923.3:n.609+175T>G
ENST00000329335.3:n.859+175T>G
ENST00000382483.3:c.609+175T>G ENSP00000371923.3:n.609+175T>G
NM_178857.5:c.609+175T>G NP_849188.4:n.609+175T>G
NM_178857.6:c.609+175T>G MANE Select NP_849188.4:n.609+175T>G
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