Canonical Allele Identifier: CA311344473
Gene: JAG1 HGNC NCBI

Linked Data

dbSNP Id: rs969179662
MyVariant Identifiers: chr20:g.10624748C>T (hg19) chr20:g.10644100C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10644100C>T , CM000682.2:g.10644100C>T GRCh38
NC_000020.10:g.10624748C>T , CM000682.1:g.10624748C>T GRCh37
NC_000020.9:g.10572748C>T NCBI36
NG_007496.1:g.34947G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254958.10:c.2373-237G>A MANE Select ENSP00000254958.4:n.2373-237G>A
ENST00000617965.2:n.2962-237G>A
ENST00000254958.9:c.2373-237G>A ENSP00000254958.4:n.2373-237G>A
ENST00000423891.6:n.2239-237G>A
NM_000214.2:c.2373-237G>A NP_000205.1:n.2373-237G>A
NM_000214.3:c.2373-237G>A MANE Select NP_000205.1:n.2373-237G>A
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