Canonical Allele Identifier: CA415269728
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349664C>A (hg19) chrX:g.151181192C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181192C>A , CM000685.2:g.151181192C>A GRCh38
NC_000023.10:g.150349664C>A , CM000685.1:g.150349664C>A GRCh37
NC_000023.9:g.150100322C>A NCBI36
NG_016405.1:g.9609C>A
NG_016405.2:g.9609C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218316.4:c.1609C>A MANE Select ENSP00000218316.3:p.Pro537Thr
ENST00000218316.3:c.1609C>A ENSP00000218316.3:p.Pro537Thr
ENST00000617907.1:c.1603C>A ENSP00000484496.1:p.Pro535Thr
NM_004224.3:c.1609C>A MANE Select NP_004215.2:p.Pro537Thr
XM_011531216.1:c.868C>A XP_011529518.1:p.Pro290Thr
XM_011531216.2:c.868C>A XP_011529518.1:p.Pro290Thr
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