Canonical Allele Identifier: CA136813391

Gene: MUC22

Linked Data

• dbSNP Id: rs890222192
• MyVariant Identifiers: chr6:g.30976606G>A (hg19) ; chr6:g.31008829G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008829G>A , CM000668.2:g.31008829G>A	GRCh38
NC_000006.11:g.30976606G>A , CM000668.1:g.30976606G>A	GRCh37
NC_000006.10:g.31084585G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-1841G>A	NP_001185744.1:n.-37-1841G>A
NM_001318484.1:c.8-1876G>A	NP_001305413.1:n.8-1876G>A