Canonical Allele Identifier: CA189306041
Gene: TYRP1 HGNC NCBI

Linked Data

dbSNP Id: rs897519629
gnomAD v4: 9-12695452-G-A
MyVariant Identifiers: chr9:g.12695452G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695452G>A , CM000671.2:g.12695452G>A GRCh38
NC_000009.11:g.12695452G>A , CM000671.1:g.12695452G>A GRCh37
NC_000009.10:g.12685452G>A NCBI36
NG_011705.1:g.7067G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.386-63G>A MANE Select ENSP00000373570.4:n.386-63G>A
ENST00000388918.9:c.386-63G>A ENSP00000373570.4:n.386-63G>A
NM_000550.2:c.386-63G>A NP_000541.1:n.386-63G>A
XR_001746372.2:n.575-63G>A
NM_000550.3:c.386-63G>A MANE Select NP_000541.1:n.386-63G>A
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