Canonical Allele Identifier: CA2201222763
Gene: MSLN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.742216A= , CM000678.2:g.742216A= GRCh38
NC_000016.9:g.792216A= , CM000678.1:g.792216A= GRCh37
NC_000016.8:g.732217A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000620831.4:c.-49-20416A= ENSP00000482893.1:n.-49-20416A=