Canonical Allele Identifier: CA826034873

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1438955664
• gnomAD v3: 6-55283161-C-G
• gnomAD v4: 6-55283161-C-G
• MyVariant Identifiers: chr6:g.55147959C>G (hg19) ; chr6:g.55283161C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+711C>G	XP_016866287.1:n.1331+711C>G