Canonical Allele Identifier: CA415269965
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349775C>T (hg19) chrX:g.151181303C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181303C>T , CM000685.2:g.151181303C>T GRCh38
NC_000023.10:g.150349775C>T , CM000685.1:g.150349775C>T GRCh37
NC_000023.9:g.150100433C>T NCBI36
NG_016405.1:g.9720C>T
NG_016405.2:g.9720C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1720C>T MANE Select ENSP00000218316.3:p.Pro574Ser
ENST00000218316.3:c.1720C>T ENSP00000218316.3:p.Pro574Ser
ENST00000617907.1:c.1714C>T ENSP00000484496.1:p.Pro572Ser
NM_004224.3:c.1720C>T MANE Select NP_004215.2:p.Pro574Ser
XM_011531216.1:c.979C>T XP_011529518.1:p.Pro327Ser
XM_011531216.2:c.979C>T XP_011529518.1:p.Pro327Ser
Search 100 bp 5'
Search 100 bp 3'