Canonical Allele Identifier: CA2122956
Community Standard Title: NM_006736.6(DNAJB2):c.366C>T (p.Pro122=)
Gene: DNAJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219282850C>T , CM000664.2:g.219282850C>T GRCh38
NC_000002.11:g.220147572C>T , CM000664.1:g.220147572C>T GRCh37
NC_000002.10:g.219855816C>T NCBI36
NG_029553.1:g.8533C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006736.6:c.366C>T MANE Select NP_006727.2:p.Pro122=
ENST00000336576.10:c.366C>T MANE Select ENSP00000338019.5:p.Pro122=
NM_001039550.1:c.366C>T NP_001034639.1:p.Pro122=
NM_001039550.2:c.366C>T NP_001034639.1:p.Pro122=
NM_006736.5:c.366C>T NP_006727.2:p.Pro122=
ENST00000336576.9:c.366C>T ENSP00000338019.5:p.Pro122=
ENST00000392086.8:c.366C>T ENSP00000375936.4:p.Pro122=
ENST00000392087.6:c.353-283C>T ENSP00000375937.2:n.353-283C>T
ENST00000425450.5:c.366C>T ENSP00000414796.1:p.Pro122=
ENST00000439026.1:c.366C>T ENSP00000387951.1:p.Pro122=
ENST00000442681.5:c.366C>T ENSP00000392790.1:p.Pro122=
ENST00000463463.5:n.357C>T
ENST00000472019.5:n.109C>T
ENST00000473750.5:n.153C>T
ENST00000477917.5:n.1584C>T
ENST00000684599.1:n.573C>T