Canonical Allele Identifier: CA2711611247
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1767232901
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283347G>C , CM000668.2:g.55283347G>C GRCh38
NC_000006.11:g.55148145G>C , CM000668.1:g.55148145G>C GRCh37
NC_000006.10:g.55256104G>C NCBI36
NG_012447.1:g.114075G>C
NG_012447.2:g.181888G>C

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+897G>C XP_016866287.1:n.1331+897G>C
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