Canonical Allele Identifier: CA566327150

Gene: MUC22

Linked Data

• dbSNP Id: rs1205564409
• gnomAD v2: 6-30976104-C-T
• gnomAD v3: 6-31008327-C-T
• gnomAD v4: 6-31008327-C-T
• MyVariant Identifiers: chr6:g.30976104C>T (hg19) ; chr6:g.31008327C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008327C>T , CM000668.2:g.31008327C>T	GRCh38
NC_000006.11:g.30976104C>T , CM000668.1:g.30976104C>T	GRCh37
NC_000006.10:g.31084083C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-38+2194C>T	NP_001185744.1:n.-38+2194C>T
NM_001318484.1:c.7+2194C>T	NP_001305413.1:n.7+2194C>T