Canonical Allele Identifier: CA139611706

Gene: HCRTR2

Linked Data

• dbSNP Id: rs150396149
• gnomAD v3: 6-55283293-C-T
• gnomAD v4: 6-55283293-C-T
• MyVariant Identifiers: chr6:g.55148091C>T (hg19) ; chr6:g.55283293C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283293C>T , CM000668.2:g.55283293C>T	GRCh38
NC_000006.11:g.55148091C>T , CM000668.1:g.55148091C>T	GRCh37
NC_000006.10:g.55256050C>T	NCBI36
NG_012447.1:g.114021C>T
NG_012447.2:g.181834C>T

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+843C>T	XP_016866287.1:n.1331+843C>T