Canonical Allele Identifier: CA1618964299
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763690932

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008885G>C , CM000668.2:g.31008885G>C GRCh38
NC_000006.11:g.30976662G>C , CM000668.1:g.30976662G>C GRCh37
NC_000006.10:g.31084641G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1785G>C NP_001185744.1:n.-37-1785G>C
NM_001318484.1:c.8-1820G>C NP_001305413.1:n.8-1820G>C