Canonical Allele Identifier: CA14205405

Gene: MSLN

Linked Data

• dbSNP Id: rs11648796
• gnomAD v2: 16-792190-A-G
• gnomAD v3: 16-742190-A-G
• gnomAD v4: 16-742190-A-G
• MyVariant Identifiers: chr16:g.792190A>G (hg19) ; chr16:g.742190A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.742190A>G , CM000678.2:g.742190A>G	GRCh38
NC_000016.9:g.792190A>G , CM000678.1:g.792190A>G	GRCh37
NC_000016.8:g.732191A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000620831.4:c.-49-20442A>G	ENSP00000482893.1:n.-49-20442A>G