Canonical Allele Identifier: CA2711418250
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs2150734909

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008575G>A , CM000668.2:g.31008575G>A GRCh38
NC_000006.11:g.30976352G>A , CM000668.1:g.30976352G>A GRCh37
NC_000006.10:g.31084331G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2095G>A NP_001185744.1:n.-37-2095G>A
NM_001318484.1:c.8-2130G>A NP_001305413.1:n.8-2130G>A