Canonical Allele Identifier: CA2398638923
Community Standard Title: NM_000496.3(CRYBB2):c.463C= (p.Gln155=)
Gene: CRYBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25231617C= , CM000684.2:g.25231617C= GRCh38
NC_000022.10:g.25627584C= , CM000684.1:g.25627584C= GRCh37
NC_000022.9:g.23957584C= NCBI36
NG_009827.1:g.16973C=

Transcript Alleles

HGVS Amino-acid Change
NM_000496.3:c.463C= MANE Select NP_000487.1:p.Gln155=
ENST00000398215.3:c.463C= MANE Select ENSP00000381273.2:p.Gln155=
NM_000496.2:c.463C= NP_000487.1:p.Gln155=
ENST00000398215.2:c.463C= ENSP00000381273.2:p.Gln155=
ENST00000651629.1:c.463C= ENSP00000498905.1:p.Gln155=
XM_006724141.2:c.463C= XP_006724204.1:p.Gln155=
XM_006724141.3:c.463C= XP_006724204.1:p.Gln155=
XM_011529900.1:c.463C= XP_011528202.1:p.Gln155=
XM_011529900.2:c.463C= XP_011528202.1:p.Gln155=
XM_011529901.1:c.463C= XP_011528203.1:p.Gln155=