Canonical Allele Identifier: CA1618964145
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008556T= , CM000668.2:g.31008556T= GRCh38
NC_000006.11:g.30976333T= , CM000668.1:g.30976333T= GRCh37
NC_000006.10:g.31084312T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2114T= NP_001185744.1:n.-37-2114T=
NM_001318484.1:c.8-2149T= NP_001305413.1:n.8-2149T=