Canonical Allele Identifier: CA139611689
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs944126598
gnomAD v3: 6-55283194-G-A
gnomAD v4: 6-55283194-G-A
MyVariant Identifiers: chr6:g.55147992G>A (hg19) chr6:g.55283194G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283194G>A , CM000668.2:g.55283194G>A GRCh38
NC_000006.11:g.55147992G>A , CM000668.1:g.55147992G>A GRCh37
NC_000006.10:g.55255951G>A NCBI36
NG_012447.1:g.113922G>A
NG_012447.2:g.181735G>A

Transcript Alleles

HGVS Amino-acid change
XM_017010798.1:c.1331+744G>A XP_016866287.1:n.1331+744G>A
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