Canonical Allele Identifier: CA2201222733
Gene: MSLN HGNC NCBI

Linked Data

dbSNP Id: rs2041399454

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.742190_742219del , CM000678.2:g.742190_742219del GRCh38
NC_000016.9:g.792190_792219del , CM000678.1:g.792190_792219del GRCh37
NC_000016.8:g.732191_732220del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000620831.4:c.-49-20442_-49-20413del ENSP00000482893.1:n.-49-20442_-49-20413del