Canonical Allele Identifier: CA139611702

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1010419441
• gnomAD v3: 6-55283266-G-T
• gnomAD v4: 6-55283266-G-T
• MyVariant Identifiers: chr6:g.55148064G>T (hg19) ; chr6:g.55283266G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283266G>T , CM000668.2:g.55283266G>T	GRCh38
NC_000006.11:g.55148064G>T , CM000668.1:g.55148064G>T	GRCh37
NC_000006.10:g.55256023G>T	NCBI36
NG_012447.1:g.113994G>T
NG_012447.2:g.181807G>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+816G>T	XP_016866287.1:n.1331+816G>T