Canonical Allele Identifier: CA1420511385
Gene: GHSR HGNC NCBI

Linked Data

dbSNP Id: rs964534167
gnomAD v4: 3-172447377-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172447377T>G , CM000665.2:g.172447377T>G GRCh38
NC_000003.11:g.172165167T>G , CM000665.1:g.172165167T>G GRCh37
NC_000003.10:g.173647861T>G NCBI36
NG_021159.1:g.6080A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.796+241A>C MANE Select ENSP00000241256.2:n.796+241A>C
ENST00000241256.2:c.796+241A>C ENSP00000241256.2:n.796+241A>C
NM_198407.2:c.796+241A>C MANE Select NP_940799.1:n.796+241A>C
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