Canonical Allele Identifier: CA357056375
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754221-C-T
MyVariant Identifiers: chr4:g.68619939C>T (hg19) chr4:g.67754221C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754221C>T , CM000666.2:g.67754221C>T GRCh38
NC_000004.11:g.68619939C>T , CM000666.1:g.68619939C>T GRCh37
NC_000004.10:g.68302534C>T NCBI36
NG_009293.1:g.6866G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.115G>A MANE Select ENSP00000226413.5:p.Val39Met
ENST00000226413.4:c.115G>A ENSP00000226413.4:p.Val39Met
ENST00000420975.2:c.115G>A ENSP00000397561.2:p.Val39Met
NM_000406.2:c.115G>A NP_000397.1:p.Val39Met
NM_001012763.1:c.115G>A NP_001012781.1:p.Val39Met
NM_000406.3:c.115G>A MANE Select NP_000397.1:p.Val39Met
NM_001012763.2:c.115G>A NP_001012781.1:p.Val39Met
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