Canonical Allele Identifier: CA477722123
Gene: JAM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134144880C>T , CM000673.2:g.134144880C>T GRCh38
NC_000011.9:g.134014775C>T , CM000673.1:g.134014775C>T GRCh37
NC_000011.8:g.133519985C>T NCBI36
NG_028348.1:g.80956C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299106.9:c.498C>T MANE Select ENSP00000299106.4:p.His166=
ENST00000299106.8:c.498C>T ENSP00000299106.4:p.His166=
ENST00000441717.3:c.345C>T ENSP00000395742.3:p.His115=
ENST00000524969.5:n.562C>T
ENST00000531302.5:n.497C>T
ENST00000532165.1:n.528C>T
ENST00000534549.5:c.318C>T ENSP00000433206.1:p.His106=
NM_001205329.1:c.345C>T NP_001192258.1:p.His115=
NM_032801.4:c.498C>T NP_116190.3:p.His166=
NM_032801.5:c.498C>T MANE Select NP_116190.3:p.His166=
NM_001205329.2:c.345C>T NP_001192258.1:p.His115=