Canonical Allele Identifier: CA136813259

Gene: MUC22

Linked Data

• dbSNP Id: rs577672623
• gnomAD v3: 6-31008314-A-T
• gnomAD v4: 6-31008314-A-T
• MyVariant Identifiers: chr6:g.30976091A>T (hg19) ; chr6:g.31008314A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008314A>T , CM000668.2:g.31008314A>T	GRCh38
NC_000006.11:g.30976091A>T , CM000668.1:g.30976091A>T	GRCh37
NC_000006.10:g.31084070A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-38+2181A>T	NP_001185744.1:n.-38+2181A>T
NM_001318484.1:c.7+2181A>T	NP_001305413.1:n.7+2181A>T