Canonical Allele Identifier: CA139611687
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs75411348
gnomAD v2: 6-55147985-A-C
gnomAD v3: 6-55283187-A-C
gnomAD v4: 6-55283187-A-C
MyVariant Identifiers: chr6:g.55147985A>C (hg19) chr6:g.55283187A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283187A>C , CM000668.2:g.55283187A>C GRCh38
NC_000006.11:g.55147985A>C , CM000668.1:g.55147985A>C GRCh37
NC_000006.10:g.55255944A>C NCBI36
NG_012447.1:g.113915A>C
NG_012447.2:g.181728A>C

Transcript Alleles

HGVS Amino-acid Change
XM_017010798.1:c.1331+737A>C XP_016866287.1:n.1331+737A>C
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