Canonical Allele Identifier: CA372936980
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695526C>G , CM000671.2:g.12695526C>G GRCh38
NC_000009.11:g.12695526C>G , CM000671.1:g.12695526C>G GRCh37
NC_000009.10:g.12685526C>G NCBI36
NG_011705.1:g.7141C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.397C>G MANE Select ENSP00000373570.4:p.Leu133Val
ENST00000388918.9:c.397C>G ENSP00000373570.4:p.Leu133Val
NM_000550.2:c.397C>G NP_000541.1:p.Leu133Val
XR_001746372.2:n.586C>G
NM_000550.3:c.397C>G MANE Select NP_000541.1:p.Leu133Val