Canonical Allele Identifier: CA1834018136
Gene: TYRP1 HGNC NCBI

Linked Data

dbSNP Id: rs1818059452
gnomAD v4: 9-12695442-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695442A>T , CM000671.2:g.12695442A>T GRCh38
NC_000009.11:g.12695442A>T , CM000671.1:g.12695442A>T GRCh37
NC_000009.10:g.12685442A>T NCBI36
NG_011705.1:g.7057A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.386-73A>T MANE Select ENSP00000373570.4:n.386-73A>T
ENST00000388918.9:c.386-73A>T ENSP00000373570.4:n.386-73A>T
NM_000550.2:c.386-73A>T NP_000541.1:n.386-73A>T
XR_001746372.2:n.575-73A>T
NM_000550.3:c.386-73A>T MANE Select NP_000541.1:n.386-73A>T