Canonical Allele Identifier: CA372937298
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695636A>G , CM000671.2:g.12695636A>G GRCh38
NC_000009.11:g.12695636A>G , CM000671.1:g.12695636A>G GRCh37
NC_000009.10:g.12685636A>G NCBI36
NG_011705.1:g.7251A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.507A>G MANE Select ENSP00000373570.4:p.Ile169Met
ENST00000388918.9:c.507A>G ENSP00000373570.4:p.Ile169Met
NM_000550.2:c.507A>G NP_000541.1:p.Ile169Met
XR_001746372.2:n.696A>G
NM_000550.3:c.507A>G MANE Select NP_000541.1:p.Ile169Met