Canonical Allele Identifier: CA415269957
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349772A>C (hg19) chrX:g.151181300A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181300A>C , CM000685.2:g.151181300A>C GRCh38
NC_000023.10:g.150349772A>C , CM000685.1:g.150349772A>C GRCh37
NC_000023.9:g.150100430A>C NCBI36
NG_016405.1:g.9717A>C
NG_016405.2:g.9717A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1717A>C MANE Select ENSP00000218316.3:p.Lys573Gln
ENST00000218316.3:c.1717A>C ENSP00000218316.3:p.Lys573Gln
ENST00000617907.1:c.1711A>C ENSP00000484496.1:p.Lys571Gln
NM_004224.3:c.1717A>C MANE Select NP_004215.2:p.Lys573Gln
XM_011531216.1:c.976A>C XP_011529518.1:p.Lys326Gln
XM_011531216.2:c.976A>C XP_011529518.1:p.Lys326Gln
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