Canonical Allele Identifier: CA415270140
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349856C>G (hg19) chrX:g.151181384C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181384C>G , CM000685.2:g.151181384C>G GRCh38
NC_000023.10:g.150349856C>G , CM000685.1:g.150349856C>G GRCh37
NC_000023.9:g.150100514C>G NCBI36
NG_016405.1:g.9801C>G
NG_016405.2:g.9801C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218316.4:c.1801C>G MANE Select ENSP00000218316.3:p.His601Asp
ENST00000218316.3:c.1801C>G ENSP00000218316.3:p.His601Asp
ENST00000617907.1:c.1795C>G ENSP00000484496.1:p.His599Asp
NM_004224.3:c.1801C>G MANE Select NP_004215.2:p.His601Asp
XM_011531216.1:c.1060C>G XP_011529518.1:p.His354Asp
XM_011531216.2:c.1060C>G XP_011529518.1:p.His354Asp
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