Canonical Allele Identifier: CA2201222750
Gene: MSLN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.742197G= , CM000678.2:g.742197G= GRCh38
NC_000016.9:g.792197G= , CM000678.1:g.792197G= GRCh37
NC_000016.8:g.732198G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000620831.4:c.-49-20435G= ENSP00000482893.1:n.-49-20435G=