Canonical Allele Identifier: CA136813409

Gene: MUC22

Linked Data

• dbSNP Id: rs894453636
• gnomAD v3: 6-31008904-TTA-T
• gnomAD v4: 6-31008904-TTA-T
• COSMIC: COSN25059238
• MyVariant Identifiers: chr6:g.30976682_30976683del (hg19) ; chr6:g.31008905_31008906del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008908_31008909del , CM000668.2:g.31008908_31008909del	GRCh38
NC_000006.11:g.30976685_30976686del , CM000668.1:g.30976685_30976686del	GRCh37
NC_000006.10:g.31084664_31084665del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-1762_-37-1761del	NP_001185744.1:n.-37-1762_-37-1761del
NM_001318484.1:c.8-1797_8-1796del	NP_001305413.1:n.8-1797_8-1796del