Canonical Allele Identifier: CA2241199678
Community Standard Title: NM_000101.4(CYBA):c.467C= (p.Pro156=)
Gene: CYBA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88643474G= , CM000678.2:g.88643474G= GRCh38
NC_000016.9:g.88709882G= , CM000678.1:g.88709882G= GRCh37
NC_000016.8:g.87237383G= NCBI36
NG_007291.1:g.12576C= , LRG_52:g.12576C=

Transcript Alleles

HGVS Amino-acid Change
NM_000101.4:c.467C= MANE Select NP_000092.2:p.Pro156=
ENST00000261623.8:c.467C= MANE Select ENSP00000261623.3:p.Pro156=
NM_000101.3:c.467C= NP_000092.2:p.Pro156=
ENST00000261623.7:c.467C= ENSP00000261623.3:p.Pro156=
ENST00000696156.1:c.383C= ENSP00000512446.1:p.Pro128=
ENST00000696157.1:c.*684C= ENSP00000512447.1:n.*684C=
ENST00000696158.1:c.*721C= ENSP00000512448.1:n.*721C=
ENST00000696159.1:c.*390C= ENSP00000512449.1:n.*390C=
ENST00000696160.1:c.494C= ENSP00000512450.1:p.Pro165=
ENST00000696161.1:c.597C= ENSP00000512451.1:p.Pro199=
ENST00000696162.1:c.*1186C= ENSP00000512452.1:n.*1186C=
ENST00000696163.1:c.416C= ENSP00000512453.1:p.Pro139=