Canonical Allele Identifier: CA439931295
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619763C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754045C>A , CM000666.2:g.67754045C>A GRCh38
NC_000004.11:g.68619763C>A , CM000666.1:g.68619763C>A GRCh37
NC_000004.10:g.68302358C>A NCBI36
NG_009293.1:g.7042G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.291G>T MANE Select ENSP00000226413.5:p.Leu97=
ENST00000226413.4:c.291G>T ENSP00000226413.4:p.Leu97=
ENST00000420975.2:c.291G>T ENSP00000397561.2:p.Leu97=
NM_000406.2:c.291G>T NP_000397.1:p.Leu97=
NM_001012763.1:c.291G>T NP_001012781.1:p.Leu97=
NM_000406.3:c.291G>T MANE Select NP_000397.1:p.Leu97=
NM_001012763.2:c.291G>T NP_001012781.1:p.Leu97=