Canonical Allele Identifier: CA2689402648
Gene: TYRP1 HGNC NCBI

Linked Data

gnomAD v4: 9-12695456-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695456T>G , CM000671.2:g.12695456T>G GRCh38
NC_000009.11:g.12695456T>G , CM000671.1:g.12695456T>G GRCh37
NC_000009.10:g.12685456T>G NCBI36
NG_011705.1:g.7071T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.386-59T>G MANE Select ENSP00000373570.4:n.386-59T>G
ENST00000388918.9:c.386-59T>G ENSP00000373570.4:n.386-59T>G
NM_000550.2:c.386-59T>G NP_000541.1:n.386-59T>G
XR_001746372.2:n.575-59T>G
NM_000550.3:c.386-59T>G MANE Select NP_000541.1:n.386-59T>G
Search 100 bp 5'
Search 100 bp 3'