Canonical Allele Identifier: CA826034856

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1240461538
• MyVariant Identifiers: chr6:g.55147923T>C (hg19) ; chr6:g.55283125T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283125T>C , CM000668.2:g.55283125T>C	GRCh38
NC_000006.11:g.55147923T>C , CM000668.1:g.55147923T>C	GRCh37
NC_000006.10:g.55255882T>C	NCBI36
NG_012447.1:g.113853T>C
NG_012447.2:g.181666T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+675T>C	XP_016866287.1:n.1331+675T>C