Canonical Allele Identifier: CA2201222694
Gene: MSLN HGNC NCBI

Linked Data

dbSNP Id: rs2041398775

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.742101T>C , CM000678.2:g.742101T>C GRCh38
NC_000016.9:g.792101T>C , CM000678.1:g.792101T>C GRCh37
NC_000016.8:g.732102T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000620831.4:c.-49-20531T>C ENSP00000482893.1:n.-49-20531T>C