Canonical Allele Identifier: CA139610896

Gene: HCRTR2

Linked Data

• dbSNP Id: rs971717928
• MyVariant Identifiers: chr6:g.55141079T>C (hg19) ; chr6:g.55276281T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55276281T>C , CM000668.2:g.55276281T>C	GRCh38
NC_000006.11:g.55141079T>C , CM000668.1:g.55141079T>C	GRCh37
NC_000006.10:g.55249038T>C	NCBI36
NG_012447.1:g.107009T>C
NG_012447.2:g.174822T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370862.4:c.763-1099T>C MANE Select	ENSP00000359899.3:n.763-1099T>C
ENST00000370862.3:c.763-1099T>C	ENSP00000359899.3:n.763-1099T>C
ENST00000615358.4:c.763-1099T>C	ENSP00000477548.1:n.763-1099T>C
NM_001526.3:c.763-1099T>C	NP_001517.2:n.763-1099T>C
XM_011514542.1:c.568-1099T>C	XP_011512844.1:n.568-1099T>C
NM_001526.4:c.763-1099T>C	NP_001517.2:n.763-1099T>C
XM_017010798.1:c.763-1099T>C	XP_016866287.1:n.763-1099T>C
NM_001384272.1:c.763-1099T>C MANE Select	NP_001371201.1:n.763-1099T>C
NM_001526.5:c.763-1099T>C	NP_001517.2:n.763-1099T>C