Canonical Allele Identifier: CA391271464
Gene: JAG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.105617048G>C (hg19) chr14:g.105150711G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.105150711G>C , CM000676.2:g.105150711G>C GRCh38
NC_000014.8:g.105617048G>C , CM000676.1:g.105617048G>C GRCh37
NC_000014.7:g.104688093G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000331782.8:c.1495C>G MANE Select ENSP00000328169.3:p.Arg499Gly
ENST00000331782.7:c.1495C>G ENSP00000328169.3:p.Arg499Gly
ENST00000347004.2:c.1381C>G ENSP00000328566.2:p.Arg461Gly
NM_002226.4:c.1495C>G NP_002217.3:p.Arg499Gly
NM_145159.2:c.1381C>G NP_660142.1:p.Arg461Gly
XM_011536736.1:c.1495C>G XP_011535038.1:p.Arg499Gly
XR_001750303.2:n.1556C>G
NM_002226.5:c.1495C>G MANE Select NP_002217.3:p.Arg499Gly
NM_145159.3:c.1381C>G NP_660142.1:p.Arg461Gly
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