Canonical Allele Identifier: CA2579301250
Gene: TYRP1 HGNC NCBI

Linked Data

gnomAD v4: 9-12695446-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695446G>A , CM000671.2:g.12695446G>A GRCh38
NC_000009.11:g.12695446G>A , CM000671.1:g.12695446G>A GRCh37
NC_000009.10:g.12685446G>A NCBI36
NG_011705.1:g.7061G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.386-69G>A MANE Select ENSP00000373570.4:n.386-69G>A
ENST00000388918.9:c.386-69G>A ENSP00000373570.4:n.386-69G>A
NM_000550.2:c.386-69G>A NP_000541.1:n.386-69G>A
XR_001746372.2:n.575-69G>A
NM_000550.3:c.386-69G>A MANE Select NP_000541.1:n.386-69G>A
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Search 100 bp 3'