Canonical Allele Identifier: CA10632391
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.12710090T>C
GRCh37 chr9:g.12710090T>C
gnomAD v2:
9:12710090 T / C
gnomAD v3:
9:12710090 T / C
gnomAD v4:
chr9-12710090-T-C
Joint Max Group AF 0.68342563 (NFE)
Genomes Max Group AF 0.68342563 (NFE)
ClinVar RCV:
RCV000313973
ClinVar Variation:
364873
dbSNP:
1063380
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12710090T>C , CM000671.2:g.12710090T>C GRCh38
NC_000009.11:g.12710090T>C , CM000671.1:g.12710090T>C GRCh37
NC_000009.10:g.12700090T>C NCBI36
NG_011705.1:g.21705T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.*908T>C (TYRP1) MANE Select ENSP00000373570.4:n.*908T>C
ENST00000388918.9:c.*908T>C (TYRP1) ENSP00000373570.4:n.*908T>C
NM_000550.2:c.*908T>C (TYRP1) NP_000541.1:n.*908T>C
NR_125775.1:n.317-9464A>G (LURAP1L-AS1)
NM_000550.3:c.*908T>C (TYRP1) MANE Select NP_000541.1:n.*908T>C
Search 100 bp 5'
Search 100 bp 3'