Canonical Allele Identifier: CA479252369

Gene: MUC19

Linked Data

• MyVariant Identifiers: chr12:g.40823447T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40429645T>G , CM000674.2:g.40429645T>G	GRCh38
NC_000012.11:g.40823447T>G , CM000674.1:g.40823447T>G	GRCh37
NC_000012.10:g.39109714T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454784.10:c.2500T>G	ENSP00000508949.1:p.Phe834Val
ENST00000454784.9:n.2546T>G
NM_173600.2:c.2500T>G	NP_775871.2:p.Phe834Val
XR_944866.1:n.75-9334A>C
XR_944867.1:n.75-9334A>C
XR_944868.1:n.75-9334A>C
XR_944869.1:n.75-9334A>C
XR_944870.1:n.75-9334A>C
XR_944871.1:n.75-9334A>C
XR_944872.1:n.81-9334A>C
XR_944873.1:n.75-9334A>C
XR_001749087.1:n.75-9334A>C
XR_001749088.1:n.75-9334A>C
XR_944868.2:n.75-9334A>C
XR_944869.2:n.75-9334A>C