Canonical Allele Identifier: CA479251658
Gene: MUC19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.40823355A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429553A>T , CM000674.2:g.40429553A>T GRCh38
NC_000012.11:g.40823355A>T , CM000674.1:g.40823355A>T GRCh37
NC_000012.10:g.39109622A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000454784.10:c.2408A>T ENSP00000508949.1:p.Asp803Val
ENST00000454784.9:n.2454A>T
NM_173600.2:c.2408A>T NP_775871.2:p.Asp803Val
XR_944866.1:n.75-9242T>A
XR_944867.1:n.75-9242T>A
XR_944868.1:n.75-9242T>A
XR_944869.1:n.75-9242T>A
XR_944870.1:n.75-9242T>A
XR_944871.1:n.75-9242T>A
XR_944872.1:n.81-9242T>A
XR_944873.1:n.75-9242T>A
XR_001749087.1:n.75-9242T>A
XR_001749088.1:n.75-9242T>A
XR_944868.2:n.75-9242T>A
XR_944869.2:n.75-9242T>A