Canonical Allele Identifier: CA837559379
Gene: GHRHR HGNC NCBI

Linked Data

dbSNP Id: rs1160953582
MyVariant Identifiers: chr7:g.31008608T>C (hg19) chr7:g.30968993T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30968993T>C , CM000669.2:g.30968993T>C GRCh38
NC_000007.13:g.31008608T>C , CM000669.1:g.31008608T>C GRCh37
NC_000007.12:g.30975133T>C NCBI36
NG_021416.1:g.9973T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000326139.7:c.160+57T>C MANE Select ENSP00000320180.2:n.160+57T>C
ENST00000326139.6:c.160+57T>C ENSP00000320180.2:n.160+57T>C
NM_000823.3:c.160+57T>C NP_000814.2:n.160+57T>C
NM_000823.4:c.160+57T>C MANE Select NP_000814.2:n.160+57T>C
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