Canonical Allele Identifier: CA2711611224
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1767230039

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283185A>G , CM000668.2:g.55283185A>G GRCh38
NC_000006.11:g.55147983A>G , CM000668.1:g.55147983A>G GRCh37
NC_000006.10:g.55255942A>G NCBI36
NG_012447.1:g.113913A>G
NG_012447.2:g.181726A>G

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+735A>G XP_016866287.1:n.1331+735A>G