Canonical Allele Identifier: CA139611681
Gene: HCRTR2 HGNC NCBI

Linked Data

dbSNP Id: rs911327497
gnomAD v2: 6-55147908-C-T
gnomAD v3: 6-55283110-C-T
gnomAD v4: 6-55283110-C-T
MyVariant Identifiers: chr6:g.55147908C>T (hg19) chr6:g.55283110C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.55283110C>T , CM000668.2:g.55283110C>T GRCh38
NC_000006.11:g.55147908C>T , CM000668.1:g.55147908C>T GRCh37
NC_000006.10:g.55255867C>T NCBI36
NG_012447.1:g.113838C>T
NG_012447.2:g.181651C>T

Transcript Alleles

HGVS Amino-acid change
XM_017010798.1:c.1331+660C>T XP_016866287.1:n.1331+660C>T
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