Canonical Allele Identifier: CA2711611233
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1767232836

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283344G>T , CM000668.2:g.55283344G>T GRCh38
NC_000006.11:g.55148142G>T , CM000668.1:g.55148142G>T GRCh37
NC_000006.10:g.55256101G>T NCBI36
NG_012447.1:g.114072G>T
NG_012447.2:g.181885G>T

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+894G>T XP_016866287.1:n.1331+894G>T