Canonical Allele Identifier: CA136813273
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs994960883

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008350A>G , CM000668.2:g.31008350A>G GRCh38
NC_000006.11:g.30976127A>G , CM000668.1:g.30976127A>G GRCh37
NC_000006.10:g.31084106A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2217A>G NP_001185744.1:n.-38+2217A>G
NM_001318484.1:c.7+2217A>G NP_001305413.1:n.7+2217A>G