Canonical Allele Identifier: CA826034884
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1262566343
MyVariant Identifiers: chr6:g.55147975C>A (hg19) chr6:g.55283177C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283177C>A , CM000668.2:g.55283177C>A GRCh38
NC_000006.11:g.55147975C>A , CM000668.1:g.55147975C>A GRCh37
NC_000006.10:g.55255934C>A NCBI36
NG_012447.1:g.113905C>A
NG_012447.2:g.181718C>A

Transcript Alleles

HGVS Amino-acid change
XM_017010798.1:c.1331+727C>A XP_016866287.1:n.1331+727C>A
Search 100 bp 5'
Search 100 bp 3'