Canonical Allele Identifier: CA357056364
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619936T>A (hg19) chr4:g.67754218T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754218T>A , CM000666.2:g.67754218T>A GRCh38
NC_000004.11:g.68619936T>A , CM000666.1:g.68619936T>A GRCh37
NC_000004.10:g.68302531T>A NCBI36
NG_009293.1:g.6869A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.118A>T MANE Select ENSP00000226413.5:p.Thr40Ser
ENST00000226413.4:c.118A>T ENSP00000226413.4:p.Thr40Ser
ENST00000420975.2:c.118A>T ENSP00000397561.2:p.Thr40Ser
NM_000406.2:c.118A>T NP_000397.1:p.Thr40Ser
NM_001012763.1:c.118A>T NP_001012781.1:p.Thr40Ser
NM_000406.3:c.118A>T MANE Select NP_000397.1:p.Thr40Ser
NM_001012763.2:c.118A>T NP_001012781.1:p.Thr40Ser
Search 100 bp 5'
Search 100 bp 3'