Canonical Allele Identifier: CA2689402649
Gene: TYRP1 HGNC NCBI

Linked Data

gnomAD v4: 9-12695457-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695457T>C , CM000671.2:g.12695457T>C GRCh38
NC_000009.11:g.12695457T>C , CM000671.1:g.12695457T>C GRCh37
NC_000009.10:g.12685457T>C NCBI36
NG_011705.1:g.7072T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.386-58T>C MANE Select ENSP00000373570.4:n.386-58T>C
ENST00000388918.9:c.386-58T>C ENSP00000373570.4:n.386-58T>C
NM_000550.2:c.386-58T>C NP_000541.1:n.386-58T>C
XR_001746372.2:n.575-58T>C
NM_000550.3:c.386-58T>C MANE Select NP_000541.1:n.386-58T>C