Canonical Allele Identifier: CA567490697
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1205359504
gnomAD v2: 6-55147898-A-T
gnomAD v3: 6-55283100-A-T
gnomAD v4: 6-55283100-A-T
MyVariant Identifiers: chr6:g.55147898A>T (hg19) chr6:g.55283100A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283100A>T , CM000668.2:g.55283100A>T GRCh38
NC_000006.11:g.55147898A>T , CM000668.1:g.55147898A>T GRCh37
NC_000006.10:g.55255857A>T NCBI36
NG_012447.1:g.113828A>T
NG_012447.2:g.181641A>T

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+650A>T XP_016866287.1:n.1331+650A>T
Search 100 bp 5'
Search 100 bp 3'