Canonical Allele Identifier: CA2839056774
Gene: GHRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30969022C>T , CM000669.2:g.30969022C>T GRCh38
NC_000007.13:g.31008637C>T , CM000669.1:g.31008637C>T GRCh37
NC_000007.12:g.30975162C>T NCBI36
NG_021416.1:g.10002C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000326139.7:c.161-41C>T MANE Select ENSP00000320180.2:n.161-41C>T
ENST00000326139.6:c.161-41C>T ENSP00000320180.2:n.161-41C>T
NM_000823.3:c.161-41C>T NP_000814.2:n.161-41C>T
NM_000823.4:c.161-41C>T MANE Select NP_000814.2:n.161-41C>T
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