Canonical Allele Identifier: CA235401050
Gene: MUC19 HGNC NCBI

Linked Data

dbSNP Id: rs1051000519

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429609A>G , CM000674.2:g.40429609A>G GRCh38
NC_000012.11:g.40823411A>G , CM000674.1:g.40823411A>G GRCh37
NC_000012.10:g.39109678A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000454784.10:c.2464A>G ENSP00000508949.1:p.Ser822Gly
ENST00000454784.9:n.2510A>G
NM_173600.2:c.2464A>G NP_775871.2:p.Ser822Gly
XR_944866.1:n.75-9298T>C
XR_944867.1:n.75-9298T>C
XR_944868.1:n.75-9298T>C
XR_944869.1:n.75-9298T>C
XR_944870.1:n.75-9298T>C
XR_944871.1:n.75-9298T>C
XR_944872.1:n.81-9298T>C
XR_944873.1:n.75-9298T>C
XR_001749087.1:n.75-9298T>C
XR_001749088.1:n.75-9298T>C
XR_944868.2:n.75-9298T>C
XR_944869.2:n.75-9298T>C