Canonical Allele Identifier: CA509816426
Gene: JAG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10639204G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10658556G>C , CM000682.2:g.10658556G>C GRCh38
NC_000020.10:g.10639204G>C , CM000682.1:g.10639204G>C GRCh37
NC_000020.9:g.10587204G>C NCBI36
NG_007496.1:g.20491C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254958.10:c.606C>G MANE Select ENSP00000254958.4:p.Pro202=
ENST00000254958.9:c.606C>G ENSP00000254958.4:p.Pro202=
ENST00000423891.6:n.472C>G
NM_000214.2:c.606C>G NP_000205.1:p.Pro202=
NM_000214.3:c.606C>G MANE Select NP_000205.1:p.Pro202=
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