Canonical Allele Identifier: CA2579301247
Gene: TYRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695437T>C , CM000671.2:g.12695437T>C GRCh38
NC_000009.11:g.12695437T>C , CM000671.1:g.12695437T>C GRCh37
NC_000009.10:g.12685437T>C NCBI36
NG_011705.1:g.7052T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.386-78T>C MANE Select ENSP00000373570.4:n.386-78T>C
ENST00000388918.9:c.386-78T>C ENSP00000373570.4:n.386-78T>C
NM_000550.2:c.386-78T>C NP_000541.1:n.386-78T>C
XR_001746372.2:n.575-78T>C
NM_000550.3:c.386-78T>C MANE Select NP_000541.1:n.386-78T>C