Canonical Allele Identifier: CA98667450

Gene: GNRHR

Linked Data

• dbSNP Id: rs1051297534
• MyVariant Identifiers: chr4:g.68606144G>A (hg19) ; chr4:g.67740426G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740426G>A , CM000666.2:g.67740426G>A	GRCh38
NC_000004.11:g.68606144G>A , CM000666.1:g.68606144G>A	GRCh37
NC_000004.10:g.68288739G>A	NCBI36
NG_009293.1:g.20661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*54C>T MANE Select	ENSP00000226413.5:n.*54C>T
ENST00000226413.4:c.*54C>T	ENSP00000226413.4:n.*54C>T
NM_000406.2:c.*54C>T	NP_000397.1:n.*54C>T
NM_001012763.1:c.*163C>T	NP_001012781.1:n.*163C>T
NM_000406.3:c.*54C>T MANE Select	NP_000397.1:n.*54C>T
NM_001012763.2:c.*163C>T	NP_001012781.1:n.*163C>T