Canonical Allele Identifier: CA1736950708
Gene: COMETT HGNC NCBI

Linked Data

dbSNP Id: rs7795356

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116576975T>G , CM000669.2:g.116576975T>G GRCh38
NC_000007.13:g.116217029T>G , CM000669.1:g.116217029T>G GRCh37
NC_000007.12:g.116004265T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120506.1:n.367-3231A>C
NR_120506.2:n.204-3231A>C
NR_165032.1:n.391-5745A>C
NR_165033.1:n.391-3231A>C