Canonical Allele Identifier: CA337198454
Gene: GPR50 HGNC NCBI

Linked Data

dbSNP Id: rs940196826
MyVariant Identifiers: chrX:g.150349780T>C (hg19) chrX:g.151181308T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181308T>C , CM000685.2:g.151181308T>C GRCh38
NC_000023.10:g.150349780T>C , CM000685.1:g.150349780T>C GRCh37
NC_000023.9:g.150100438T>C NCBI36
NG_016405.1:g.9725T>C
NG_016405.2:g.9725T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1725T>C MANE Select ENSP00000218316.3:p.Ala575=
ENST00000218316.3:c.1725T>C ENSP00000218316.3:p.Ala575=
ENST00000617907.1:c.1719T>C ENSP00000484496.1:p.Ala573=
NM_004224.3:c.1725T>C MANE Select NP_004215.2:p.Ala575=
XM_011531216.1:c.984T>C XP_011529518.1:p.Ala328=
XM_011531216.2:c.984T>C XP_011529518.1:p.Ala328=
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