Canonical Allele Identifier: CA826034882
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs80205887
MyVariant Identifiers: chr6:g.55147964T>C (hg19) chr6:g.55283166T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283166T>C , CM000668.2:g.55283166T>C GRCh38
NC_000006.11:g.55147964T>C , CM000668.1:g.55147964T>C GRCh37
NC_000006.10:g.55255923T>C NCBI36
NG_012447.1:g.113894T>C
NG_012447.2:g.181707T>C

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+716T>C XP_016866287.1:n.1331+716T>C
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