Canonical Allele Identifier: CA6515288
Gene: MUC19 HGNC NCBI

Linked Data

dbSNP Id: rs11564245

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429552G>C , CM000674.2:g.40429552G>C GRCh38
NC_000012.11:g.40823354G>C , CM000674.1:g.40823354G>C GRCh37
NC_000012.10:g.39109621G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000454784.10:c.2407G>C ENSP00000508949.1:p.Asp803His
ENST00000454784.9:n.2453G>C
NM_173600.2:c.2407G>C NP_775871.2:p.Asp803His
XR_944866.1:n.75-9241C>G
XR_944867.1:n.75-9241C>G
XR_944868.1:n.75-9241C>G
XR_944869.1:n.75-9241C>G
XR_944870.1:n.75-9241C>G
XR_944871.1:n.75-9241C>G
XR_944872.1:n.81-9241C>G
XR_944873.1:n.75-9241C>G
XR_001749087.1:n.75-9241C>G
XR_001749088.1:n.75-9241C>G
XR_944868.2:n.75-9241C>G
XR_944869.2:n.75-9241C>G