Canonical Allele Identifier: CA139611710
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1022147189
gnomAD v2: 6-55148102-G-A
gnomAD v3: 6-55283304-G-A
gnomAD v4: 6-55283304-G-A
MyVariant Identifiers: chr6:g.55148102G>A (hg19) chr6:g.55283304G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283304G>A , CM000668.2:g.55283304G>A GRCh38
NC_000006.11:g.55148102G>A , CM000668.1:g.55148102G>A GRCh37
NC_000006.10:g.55256061G>A NCBI36
NG_012447.1:g.114032G>A
NG_012447.2:g.181845G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+854G>A XP_016866287.1:n.1331+854G>A
Search 100 bp 5'
Search 100 bp 3'