Canonical Allele Identifier: CA479251759
Gene: MUC19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.40823368T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40429566T>C , CM000674.2:g.40429566T>C GRCh38
NC_000012.11:g.40823368T>C , CM000674.1:g.40823368T>C GRCh37
NC_000012.10:g.39109635T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000454784.10:c.2421T>C ENSP00000508949.1:p.Ser807=
ENST00000454784.9:n.2467T>C
NM_173600.2:c.2421T>C NP_775871.2:p.Ser807=
XR_944866.1:n.75-9255A>G
XR_944867.1:n.75-9255A>G
XR_944868.1:n.75-9255A>G
XR_944869.1:n.75-9255A>G
XR_944870.1:n.75-9255A>G
XR_944871.1:n.75-9255A>G
XR_944872.1:n.81-9255A>G
XR_944873.1:n.75-9255A>G
XR_001749087.1:n.75-9255A>G
XR_001749088.1:n.75-9255A>G
XR_944868.2:n.75-9255A>G
XR_944869.2:n.75-9255A>G
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