Canonical Allele Identifier: CA797723911
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs1340962298
MyVariant Identifiers: chr4:g.68797691C>G (hg19) chr4:g.67931973C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931973C>G , CM000666.2:g.67931973C>G GRCh38
NC_000004.11:g.68797691C>G , CM000666.1:g.68797691C>G GRCh37
NC_000004.10:g.68480286C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.320+20G>C MANE Select ENSP00000426911.2:n.320+20G>C
ENST00000334830.11:c.329+20G>C ENSP00000334611.7:n.329+20G>C
ENST00000396188.3:c.320+20G>C ENSP00000379491.3:n.320+20G>C
ENST00000508048.5:c.320+20G>C ENSP00000426911.2:n.320+20G>C
ENST00000513536.5:c.260+20G>C ENSP00000427621.1:n.260+20G>C
NM_001114387.1:c.320+20G>C NP_001107859.1:n.320+20G>C
NM_182606.3:c.329+20G>C NP_872412.3:n.329+20G>C
NM_001114387.2:c.320+20G>C MANE Select NP_001107859.1:n.320+20G>C
NM_182606.4:c.329+20G>C NP_872412.3:n.329+20G>C
Search 100 bp 5'
Search 100 bp 3'