Canonical Allele Identifier: CA1618964143
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763659843

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008555_31008556insCT , CM000668.2:g.31008555_31008556insCT GRCh38
NC_000006.11:g.30976332_30976333insCT , CM000668.1:g.30976332_30976333insCT GRCh37
NC_000006.10:g.31084311_31084312insCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2115_-37-2114insCT NP_001185744.1:n.-37-2115_-37-2114insCT
NM_001318484.1:c.8-2150_8-2149insCT NP_001305413.1:n.8-2150_8-2149insCT