Canonical Allele Identifier: CA139611698
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs906159964
gnomAD v2: 6-55148051-A-G
gnomAD v3: 6-55283253-A-G
gnomAD v4: 6-55283253-A-G
MyVariant Identifiers: chr6:g.55148051A>G (hg19) chr6:g.55283253A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283253A>G , CM000668.2:g.55283253A>G GRCh38
NC_000006.11:g.55148051A>G , CM000668.1:g.55148051A>G GRCh37
NC_000006.10:g.55256010A>G NCBI36
NG_012447.1:g.113981A>G
NG_012447.2:g.181794A>G

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+803A>G XP_016866287.1:n.1331+803A>G
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