Canonical Allele Identifier: CA450593416
Gene: HCRTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.55113444G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55248646G>A , CM000668.2:g.55248646G>A GRCh38
NC_000006.11:g.55113444G>A , CM000668.1:g.55113444G>A GRCh37
NC_000006.10:g.55221403G>A NCBI36
NG_012447.1:g.79374G>A
NG_012447.2:g.147187G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370862.4:c.231G>A MANE Select ENSP00000359899.3:p.Val77=
ENST00000370862.3:c.231G>A ENSP00000359899.3:p.Val77=
ENST00000615358.4:c.231G>A ENSP00000477548.1:p.Val77=
NM_001526.3:c.231G>A NP_001517.2:p.Val77=
XM_011514542.1:c.36G>A XP_011512844.1:p.Val12=
NM_001526.4:c.231G>A NP_001517.2:p.Val77=
XM_017010798.1:c.231G>A XP_016866287.1:p.Val77=
NM_001384272.1:c.231G>A MANE Select NP_001371201.1:p.Val77=
NM_001526.5:c.231G>A NP_001517.2:p.Val77=
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