Canonical Allele Identifier: CA139599365
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs964509464
MyVariant Identifiers: chr6:g.55045101A>G (hg19) chr6:g.55180303A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55180303A>G , CM000668.2:g.55180303A>G GRCh38
NC_000006.11:g.55045101A>G , CM000668.1:g.55045101A>G GRCh37
NC_000006.10:g.55153060A>G NCBI36
NG_012447.1:g.11031A>G
NG_012447.2:g.78844A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.223+5493A>G MANE Select ENSP00000359899.3:n.223+5493A>G
ENST00000370862.3:c.223+5493A>G ENSP00000359899.3:n.223+5493A>G
ENST00000615358.4:c.223+5493A>G ENSP00000477548.1:n.223+5493A>G
NM_001526.3:c.223+5493A>G NP_001517.2:n.223+5493A>G
NM_001526.4:c.223+5493A>G NP_001517.2:n.223+5493A>G
XM_017010798.1:c.223+5493A>G XP_016866287.1:n.223+5493A>G
NM_001384272.1:c.223+5493A>G MANE Select NP_001371201.1:n.223+5493A>G
NM_001526.5:c.223+5493A>G NP_001517.2:n.223+5493A>G
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