Canonical Allele Identifier: CA515669232
Community Standard Title: NM_000397.4(CYBB):c.252G>C (p.Ala84=)
Gene: CYBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.37783600G>C , CM000685.2:g.37783600G>C GRCh38
NC_000023.10:g.37642853G>C , CM000685.1:g.37642853G>C GRCh37
NC_000023.9:g.37527797G>C NCBI36
NG_009065.1:g.8584G>C , LRG_53:g.8584G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000397.4:c.252G>C MANE Select NP_000388.2:p.Ala84=
ENST00000378588.5:c.252G>C MANE Select ENSP00000367851.4:p.Ala84=
NM_000397.3:c.252G>C , LRG_53t1:c.252G>C NP_000388.2:p.Ala84=
ENST00000378588.4:c.252G>C ENSP00000367851.4:p.Ala84=
ENST00000465127.1:c.171+357600G>C ENSP00000417050.1:n.171+357600G>C
ENST00000696170.1:c.252G>C ENSP00000512461.1:p.Ala84=
ENST00000696171.1:c.156G>C ENSP00000512462.1:p.Ala52=
ENST00000696172.1:c.252G>C ENSP00000512463.1:p.Ala84=
ENST00000696173.1:n.260G>C
XM_011543890.1:c.-179G>C XP_011542192.1:n.-179G>C