Canonical Allele Identifier: CA2711611206
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1767229068
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283134A>T , CM000668.2:g.55283134A>T GRCh38
NC_000006.11:g.55147932A>T , CM000668.1:g.55147932A>T GRCh37
NC_000006.10:g.55255891A>T NCBI36
NG_012447.1:g.113862A>T
NG_012447.2:g.181675A>T

Transcript Alleles

HGVS Amino-acid change
XM_017010798.1:c.1331+684A>T XP_016866287.1:n.1331+684A>T
Search 100 bp 5'
Search 100 bp 3'