Canonical Allele Identifier: CA1618964075
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763646171

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008392G>A , CM000668.2:g.31008392G>A GRCh38
NC_000006.11:g.30976169G>A , CM000668.1:g.30976169G>A GRCh37
NC_000006.10:g.31084148G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2259G>A NP_001185744.1:n.-38+2259G>A
NM_001318484.1:c.7+2259G>A NP_001305413.1:n.7+2259G>A