Canonical Allele Identifier: CA826034869

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1344429205
• gnomAD v3: 6-55283133-T-C
• gnomAD v4: 6-55283133-T-C
• MyVariant Identifiers: chr6:g.55147931T>C (hg19) ; chr6:g.55283133T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283133T>C , CM000668.2:g.55283133T>C	GRCh38
NC_000006.11:g.55147931T>C , CM000668.1:g.55147931T>C	GRCh37
NC_000006.10:g.55255890T>C	NCBI36
NG_012447.1:g.113861T>C
NG_012447.2:g.181674T>C

Transcript Alleles

HGVS	Amino-acid change
XM_017010798.1:c.1331+683T>C	XP_016866287.1:n.1331+683T>C