Canonical Allele Identifier: CA139611691

Gene: HCRTR2

Linked Data

• dbSNP Id: rs538277125
• gnomAD v3: 6-55283205-C-A
• gnomAD v4: 6-55283205-C-A
• MyVariant Identifiers: chr6:g.55148003C>A (hg19) ; chr6:g.55283205C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283205C>A , CM000668.2:g.55283205C>A	GRCh38
NC_000006.11:g.55148003C>A , CM000668.1:g.55148003C>A	GRCh37
NC_000006.10:g.55255962C>A	NCBI36
NG_012447.1:g.113933C>A
NG_012447.2:g.181746C>A

Transcript Alleles

HGVS	Amino-acid change
XM_017010798.1:c.1331+755C>A	XP_016866287.1:n.1331+755C>A