Canonical Allele Identifier: CA479265178

Gene: MUC19

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40441116C>A , CM000674.2:g.40441116C>A	GRCh38
NC_000012.11:g.40834918C>A , CM000674.1:g.40834918C>A	GRCh37
NC_000012.10:g.39121185C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454784.10:c.3677C>A	ENSP00000508949.1:p.Ser1226Tyr
ENST00000454784.9:n.3723C>A
NM_173600.2:c.3677C>A	NP_775871.2:p.Ser1226Tyr
XR_944866.1:n.74+2707G>T
XR_944867.1:n.74+2707G>T
XR_944868.1:n.74+2707G>T
XR_944869.1:n.74+2707G>T
XR_944870.1:n.74+2707G>T
XR_944871.1:n.74+2707G>T
XR_944872.1:n.35G>T
XR_944873.1:n.74+2707G>T
XR_001749087.1:n.74+2707G>T
XR_001749088.1:n.74+2707G>T
XR_944868.2:n.74+2707G>T
XR_944869.2:n.74+2707G>T