Canonical Allele Identifier: CA567490914

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1342504788
• gnomAD v2: 6-55148075-G-C
• gnomAD v3: 6-55283277-G-C
• gnomAD v4: 6-55283277-G-C
• MyVariant Identifiers: chr6:g.55148075G>C (hg19) ; chr6:g.55283277G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283277G>C , CM000668.2:g.55283277G>C	GRCh38
NC_000006.11:g.55148075G>C , CM000668.1:g.55148075G>C	GRCh37
NC_000006.10:g.55256034G>C	NCBI36
NG_012447.1:g.114005G>C
NG_012447.2:g.181818G>C

Transcript Alleles

HGVS	Amino-acid change
XM_017010798.1:c.1331+827G>C	XP_016866287.1:n.1331+827G>C