Canonical Allele Identifier: CA139599353
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1031861202
MyVariant Identifiers: chr6:g.55045019C>A (hg19) chr6:g.55180221C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55180221C>A , CM000668.2:g.55180221C>A GRCh38
NC_000006.11:g.55045019C>A , CM000668.1:g.55045019C>A GRCh37
NC_000006.10:g.55152978C>A NCBI36
NG_012447.1:g.10949C>A
NG_012447.2:g.78762C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370862.4:c.223+5411C>A MANE Select ENSP00000359899.3:n.223+5411C>A
ENST00000370862.3:c.223+5411C>A ENSP00000359899.3:n.223+5411C>A
ENST00000615358.4:c.223+5411C>A ENSP00000477548.1:n.223+5411C>A
NM_001526.3:c.223+5411C>A NP_001517.2:n.223+5411C>A
NM_001526.4:c.223+5411C>A NP_001517.2:n.223+5411C>A
XM_017010798.1:c.223+5411C>A XP_016866287.1:n.223+5411C>A
NM_001384272.1:c.223+5411C>A MANE Select NP_001371201.1:n.223+5411C>A
NM_001526.5:c.223+5411C>A NP_001517.2:n.223+5411C>A
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