Canonical Allele Identifier: CA136813368

Gene: MUC22

Linked Data

• dbSNP Id: rs34809789
• MyVariant Identifiers: chr6:g.30976479C>A (hg19) ; chr6:g.31008702C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008702C>A , CM000668.2:g.31008702C>A	GRCh38
NC_000006.11:g.30976479C>A , CM000668.1:g.30976479C>A	GRCh37
NC_000006.10:g.31084458C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-1968C>A	NP_001185744.1:n.-37-1968C>A
NM_001318484.1:c.8-2003C>A	NP_001305413.1:n.8-2003C>A