Canonical Allele Identifier: CA1618964233
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763676494

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008714A>G , CM000668.2:g.31008714A>G GRCh38
NC_000006.11:g.30976491A>G , CM000668.1:g.30976491A>G GRCh37
NC_000006.10:g.31084470A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1956A>G NP_001185744.1:n.-37-1956A>G
NM_001318484.1:c.8-1991A>G NP_001305413.1:n.8-1991A>G