Canonical Allele Identifier: CA826034872

Gene: HCRTR2

Linked Data

• dbSNP Id: rs1275479138
• gnomAD v3: 6-55283148-A-C
• gnomAD v4: 6-55283148-A-C
• MyVariant Identifiers: chr6:g.55147946A>C (hg19) ; chr6:g.55283148A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55283148A>C , CM000668.2:g.55283148A>C	GRCh38
NC_000006.11:g.55147946A>C , CM000668.1:g.55147946A>C	GRCh37
NC_000006.10:g.55255905A>C	NCBI36
NG_012447.1:g.113876A>C
NG_012447.2:g.181689A>C

Transcript Alleles

HGVS	Amino-acid Change
XM_017010798.1:c.1331+698A>C	XP_016866287.1:n.1331+698A>C