Canonical Allele Identifier: CA826034943

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1238560985
• MyVariant Identifiers: chr6:g.55148069A>C (hg19) ; chr6:g.55283271A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283271A>C , CM000668.2:g.55283271A>C	GRCh38
NC_000006.11:g.55148069A>C , CM000668.1:g.55148069A>C	GRCh37
NC_000006.10:g.55256028A>C	NCBI36
NG_012447.1:g.113999A>C
NG_012447.2:g.181812A>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+821A>C	XP_016866287.1:n.1331+821A>C