Canonical Allele Identifier: CA479252315

Gene: MUC19

Linked Data

• dbSNP Id: rs1417621621
• gnomAD v3: 12-40429639-T-C
• gnomAD v4: 12-40429639-T-C
• MyVariant Identifiers: chr12:g.40823441T>C (hg19) ; chr12:g.40429639T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40429639T>C , CM000674.2:g.40429639T>C	GRCh38
NC_000012.11:g.40823441T>C , CM000674.1:g.40823441T>C	GRCh37
NC_000012.10:g.39109708T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454784.10:c.2494T>C	ENSP00000508949.1:p.Tyr832His
ENST00000454784.9:n.2540T>C
NM_173600.2:c.2494T>C	NP_775871.2:p.Tyr832His
XR_944866.1:n.75-9328A>G
XR_944867.1:n.75-9328A>G
XR_944868.1:n.75-9328A>G
XR_944869.1:n.75-9328A>G
XR_944870.1:n.75-9328A>G
XR_944871.1:n.75-9328A>G
XR_944872.1:n.81-9328A>G
XR_944873.1:n.75-9328A>G
XR_001749087.1:n.75-9328A>G
XR_001749088.1:n.75-9328A>G
XR_944868.2:n.75-9328A>G
XR_944869.2:n.75-9328A>G