Canonical Allele Identifier: CA823869711
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1241340714

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008352G>A , CM000668.2:g.31008352G>A GRCh38
NC_000006.11:g.30976129G>A , CM000668.1:g.30976129G>A GRCh37
NC_000006.10:g.31084108G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2219G>A NP_001185744.1:n.-38+2219G>A
NM_001318484.1:c.7+2219G>A NP_001305413.1:n.7+2219G>A