Canonical Allele Identifier: CA2313988711
Gene: CYB5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.74280957A= , CM000680.2:g.74280957A= GRCh38
NC_000018.9:g.71948192A= , CM000680.1:g.71948192A= GRCh37
NC_000018.8:g.70099172A= NCBI36
NG_023211.1:g.16030T=

Transcript Alleles

HGVS Amino-acid change
ENST00000340533.9:c.129+10790T= MANE Select ENSP00000341625.4:n.129+10790T=
ENST00000299438.13:c.-94+9931T= ENSP00000299438.9:n.-94+9931T=
ENST00000340533.8:c.129+10790T= ENSP00000341625.4:n.129+10790T=
ENST00000397914.4:c.129+10790T= ENSP00000381011.4:n.129+10790T=
ENST00000494131.6:c.129+10790T= ENSP00000436461.2:n.129+10790T=
ENST00000583418.1:n.211+10790T=
NM_001190807.2:c.129+10790T= NP_001177736.1:n.129+10790T=
NM_001914.3:c.129+10790T= NP_001905.1:n.129+10790T=
NM_148923.3:c.129+10790T= NP_683725.1:n.129+10790T=
XM_011525835.1:c.129+10790T= XP_011524137.1:n.129+10790T=
XM_011525835.2:c.129+10790T= XP_011524137.1:n.129+10790T=
NM_148923.4:c.129+10790T= MANE Select NP_683725.1:n.129+10790T=
NM_001190807.3:c.129+10790T= NP_001177736.1:n.129+10790T=
NM_001914.4:c.129+10790T= NP_001905.1:n.129+10790T=