Canonical Allele Identifier: CA454286127
Gene: GHRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.31008487C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30968872C>G , CM000669.2:g.30968872C>G GRCh38
NC_000007.13:g.31008487C>G , CM000669.1:g.31008487C>G GRCh37
NC_000007.12:g.30975012C>G NCBI36
NG_021416.1:g.9852C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000326139.7:c.96C>G MANE Select ENSP00000320180.2:p.Thr32=
ENST00000326139.6:c.96C>G ENSP00000320180.2:p.Thr32=
ENST00000466427.1:n.323C>G
NM_000823.3:c.96C>G NP_000814.2:p.Thr32=
NM_000823.4:c.96C>G MANE Select NP_000814.2:p.Thr32=
Search 100 bp 5'
Search 100 bp 3'