Canonical Allele Identifier: CA355514529
Gene: GHSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447989T>C , CM000665.2:g.172447989T>C GRCh38
NC_000003.11:g.172165779T>C , CM000665.1:g.172165779T>C GRCh37
NC_000003.10:g.173648473T>C NCBI36
NG_021159.1:g.5468A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.425A>G MANE Select ENSP00000241256.2:p.Tyr142Cys
ENST00000241256.2:c.425A>G ENSP00000241256.2:p.Tyr142Cys
ENST00000427970.1:c.425A>G ENSP00000395344.1:p.Tyr142Cys
NM_004122.2:c.425A>G NP_004113.1:p.Tyr142Cys
NM_198407.2:c.425A>G MANE Select NP_940799.1:p.Tyr142Cys