Canonical Allele Identifier: CA2597584036
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1767233082
gnomAD v3: 6-55283362-T-C
gnomAD v4: 6-55283362-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283362T>C , CM000668.2:g.55283362T>C GRCh38
NC_000006.11:g.55148160T>C , CM000668.1:g.55148160T>C GRCh37
NC_000006.10:g.55256119T>C NCBI36
NG_012447.1:g.114090T>C
NG_012447.2:g.181903T>C

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+912T>C XP_016866287.1:n.1331+912T>C
Search 100 bp 5'
Search 100 bp 3'