Canonical Allele Identifier: CA1618964243
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008742A= , CM000668.2:g.31008742A= GRCh38
NC_000006.11:g.30976519A= , CM000668.1:g.30976519A= GRCh37
NC_000006.10:g.31084498A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1928A= NP_001185744.1:n.-37-1928A=
NM_001318484.1:c.8-1963A= NP_001305413.1:n.8-1963A=