Canonical Allele Identifier: CA2031018822
Gene: MUC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429278A= , CM000674.2:g.40429278A= GRCh38
NC_000012.11:g.40823080A= , CM000674.1:g.40823080A= GRCh37
NC_000012.10:g.39109347A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454784.10:c.2397-264A= ENSP00000508949.1:n.2397-264A=
ENST00000454784.9:n.2443-264A=
NM_173600.2:c.2397-264A= NP_775871.2:n.2397-264A=
XR_944866.1:n.75-8967T=
XR_944867.1:n.75-8967T=
XR_944868.1:n.75-8967T=
XR_944869.1:n.75-8967T=
XR_944870.1:n.75-8967T=
XR_944871.1:n.75-8967T=
XR_944872.1:n.81-8967T=
XR_944873.1:n.75-8967T=
XR_001749087.1:n.75-8967T=
XR_001749088.1:n.75-8967T=
XR_944868.2:n.75-8967T=
XR_944869.2:n.75-8967T=