Canonical Allele Identifier: CA439933872
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68619931A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754213A>T , CM000666.2:g.67754213A>T GRCh38
NC_000004.11:g.68619931A>T , CM000666.1:g.68619931A>T GRCh37
NC_000004.10:g.68302526A>T NCBI36
NG_009293.1:g.6874T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.123T>A MANE Select ENSP00000226413.5:p.Val41=
ENST00000226413.4:c.123T>A ENSP00000226413.4:p.Val41=
ENST00000420975.2:c.123T>A ENSP00000397561.2:p.Val41=
NM_000406.2:c.123T>A NP_000397.1:p.Val41=
NM_001012763.1:c.123T>A NP_001012781.1:p.Val41=
NM_000406.3:c.123T>A MANE Select NP_000397.1:p.Val41=
NM_001012763.2:c.123T>A NP_001012781.1:p.Val41=
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Search 100 bp 3'