Canonical Allele Identifier: CA364609020
Gene: HCRTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.55113439T>A (hg19) chr6:g.55248641T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248641T>A , CM000668.2:g.55248641T>A GRCh38
NC_000006.11:g.55113439T>A , CM000668.1:g.55113439T>A GRCh37
NC_000006.10:g.55221398T>A NCBI36
NG_012447.1:g.79369T>A
NG_012447.2:g.147182T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370862.4:c.226T>A MANE Select ENSP00000359899.3:p.Cys76Ser
ENST00000370862.3:c.226T>A ENSP00000359899.3:p.Cys76Ser
ENST00000615358.4:c.226T>A ENSP00000477548.1:p.Cys76Ser
NM_001526.3:c.226T>A NP_001517.2:p.Cys76Ser
XM_011514542.1:c.31T>A XP_011512844.1:p.Cys11Ser
NM_001526.4:c.226T>A NP_001517.2:p.Cys76Ser
XM_017010798.1:c.226T>A XP_016866287.1:p.Cys76Ser
NM_001384272.1:c.226T>A MANE Select NP_001371201.1:p.Cys76Ser
NM_001526.5:c.226T>A NP_001517.2:p.Cys76Ser
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