Canonical Allele Identifier: CA1089213320
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1438955664
gnomAD v3: 6-55283161-C-A
gnomAD v4: 6-55283161-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283161C>A , CM000668.2:g.55283161C>A GRCh38
NC_000006.11:g.55147959C>A , CM000668.1:g.55147959C>A GRCh37
NC_000006.10:g.55255918C>A NCBI36
NG_012447.1:g.113889C>A
NG_012447.2:g.181702C>A

Transcript Alleles

HGVS Amino-acid change
XM_017010798.1:c.1331+711C>A XP_016866287.1:n.1331+711C>A
Search 100 bp 5'
Search 100 bp 3'