Canonical Allele Identifier: CA1618964081
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1581592026

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008401A>G , CM000668.2:g.31008401A>G GRCh38
NC_000006.11:g.30976178A>G , CM000668.1:g.30976178A>G GRCh37
NC_000006.10:g.31084157A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2269A>G NP_001185744.1:n.-37-2269A>G
NM_001318484.1:c.7+2268A>G NP_001305413.1:n.7+2268A>G