Canonical Allele Identifier: CA355514424
Gene: GHSR HGNC NCBI

Linked Data

gnomAD v4: 3-172447958-C-A
MyVariant Identifiers: chr3:g.172165748C>A (hg19) chr3:g.172447958C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447958C>A , CM000665.2:g.172447958C>A GRCh38
NC_000003.11:g.172165748C>A , CM000665.1:g.172165748C>A GRCh37
NC_000003.10:g.173648442C>A NCBI36
NG_021159.1:g.5499G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000241256.3:c.456G>T MANE Select ENSP00000241256.2:p.Lys152Asn
ENST00000241256.2:c.456G>T ENSP00000241256.2:p.Lys152Asn
ENST00000427970.1:c.456G>T ENSP00000395344.1:p.Lys152Asn
NM_004122.2:c.456G>T NP_004113.1:p.Lys152Asn
NM_198407.2:c.456G>T MANE Select NP_940799.1:p.Lys152Asn
Search 100 bp 5'
Search 100 bp 3'