Canonical Allele Identifier: CA139610881
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs2173993
MyVariant Identifiers: chr6:g.55140890G>C (hg19) chr6:g.55276092G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55276092G>C , CM000668.2:g.55276092G>C GRCh38
NC_000006.11:g.55140890G>C , CM000668.1:g.55140890G>C GRCh37
NC_000006.10:g.55248849G>C NCBI36
NG_012447.1:g.106820G>C
NG_012447.2:g.174633G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370862.4:c.763-1288G>C MANE Select ENSP00000359899.3:n.763-1288G>C
ENST00000370862.3:c.763-1288G>C ENSP00000359899.3:n.763-1288G>C
ENST00000615358.4:c.763-1288G>C ENSP00000477548.1:n.763-1288G>C
NM_001526.3:c.763-1288G>C NP_001517.2:n.763-1288G>C
XM_011514542.1:c.568-1288G>C XP_011512844.1:n.568-1288G>C
NM_001526.4:c.763-1288G>C NP_001517.2:n.763-1288G>C
XM_017010798.1:c.763-1288G>C XP_016866287.1:n.763-1288G>C
NM_001384272.1:c.763-1288G>C MANE Select NP_001371201.1:n.763-1288G>C
NM_001526.5:c.763-1288G>C NP_001517.2:n.763-1288G>C
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