Canonical Allele Identifier: CA1087405761
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763663830

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008593G>T , CM000668.2:g.31008593G>T GRCh38
NC_000006.11:g.30976370G>T , CM000668.1:g.30976370G>T GRCh37
NC_000006.10:g.31084349G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2077G>T NP_001185744.1:n.-37-2077G>T
NM_001318484.1:c.8-2112G>T NP_001305413.1:n.8-2112G>T