Canonical Allele Identifier: CA2579301246
Gene: TYRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695432G>A , CM000671.2:g.12695432G>A GRCh38
NC_000009.11:g.12695432G>A , CM000671.1:g.12695432G>A GRCh37
NC_000009.10:g.12685432G>A NCBI36
NG_011705.1:g.7047G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.386-83G>A MANE Select ENSP00000373570.4:n.386-83G>A
ENST00000388918.9:c.386-83G>A ENSP00000373570.4:n.386-83G>A
NM_000550.2:c.386-83G>A NP_000541.1:n.386-83G>A
XR_001746372.2:n.575-83G>A
NM_000550.3:c.386-83G>A MANE Select NP_000541.1:n.386-83G>A