Canonical Allele Identifier: CA355516823
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs1359269872
gnomAD v2: 3-172166149-G-T
gnomAD v4: 3-172448359-G-T
MyVariant Identifiers: chr3:g.172166149G>T (hg19) chr3:g.172448359G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448359G>T , CM000665.2:g.172448359G>T GRCh38
NC_000003.11:g.172166149G>T , CM000665.1:g.172166149G>T GRCh37
NC_000003.10:g.173648843G>T NCBI36
NG_021159.1:g.5098C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.55C>A MANE Select ENSP00000241256.2:p.Leu19Met
ENST00000241256.2:c.55C>A ENSP00000241256.2:p.Leu19Met
ENST00000427970.1:c.55C>A ENSP00000395344.1:p.Leu19Met
NM_004122.2:c.55C>A NP_004113.1:p.Leu19Met
NM_198407.2:c.55C>A MANE Select NP_940799.1:p.Leu19Met
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