Canonical Allele Identifier: CA436965610
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172166060G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448270G>C , CM000665.2:g.172448270G>C GRCh38
NC_000003.11:g.172166060G>C , CM000665.1:g.172166060G>C GRCh37
NC_000003.10:g.173648754G>C NCBI36
NG_021159.1:g.5187C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.144C>G MANE Select ENSP00000241256.2:p.Ala48=
ENST00000241256.2:c.144C>G ENSP00000241256.2:p.Ala48=
ENST00000427970.1:c.144C>G ENSP00000395344.1:p.Ala48=
NM_004122.2:c.144C>G NP_004113.1:p.Ala48=
NM_198407.2:c.144C>G MANE Select NP_940799.1:p.Ala48=