Canonical Allele Identifier: CA860106327
Gene: TYRP1 HGNC NCBI

Linked Data

dbSNP Id: rs1327321630
MyVariant Identifiers: chr9:g.12695453C>T (hg19) chr9:g.12695453C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695453C>T , CM000671.2:g.12695453C>T GRCh38
NC_000009.11:g.12695453C>T , CM000671.1:g.12695453C>T GRCh37
NC_000009.10:g.12685453C>T NCBI36
NG_011705.1:g.7068C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.386-62C>T MANE Select ENSP00000373570.4:n.386-62C>T
ENST00000388918.9:c.386-62C>T ENSP00000373570.4:n.386-62C>T
NM_000550.2:c.386-62C>T NP_000541.1:n.386-62C>T
XR_001746372.2:n.575-62C>T
NM_000550.3:c.386-62C>T MANE Select NP_000541.1:n.386-62C>T
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