Canonical Allele Identifier: CA946837695
Gene: MUC19 HGNC NCBI

Linked Data

dbSNP Id: rs1947901560

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429134dup , CM000674.2:g.40429134dup GRCh38
NC_000012.11:g.40822936dup , CM000674.1:g.40822936dup GRCh37
NC_000012.10:g.39109203dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454784.10:c.2397-408dup ENSP00000508949.1:n.2397-408dup
ENST00000454784.9:n.2443-408dup
NM_173600.2:c.2397-408dup NP_775871.2:n.2397-408dup
XR_944866.1:n.75-8820dup
XR_944867.1:n.75-8820dup
XR_944868.1:n.75-8820dup
XR_944869.1:n.75-8820dup
XR_944870.1:n.75-8820dup
XR_944871.1:n.75-8820dup
XR_944872.1:n.81-8820dup
XR_944873.1:n.75-8820dup
XR_001749087.1:n.75-8820dup
XR_001749088.1:n.75-8820dup
XR_944868.2:n.75-8820dup
XR_944869.2:n.75-8820dup