Canonical Allele Identifier: CA10158041
Gene: CRYBB2 HGNC NCBI

Linked Data

dbSNP Id: rs757433401

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25231621A>G , CM000684.2:g.25231621A>G GRCh38
NC_000022.10:g.25627588A>G , CM000684.1:g.25627588A>G GRCh37
NC_000022.9:g.23957588A>G NCBI36
NG_009827.1:g.16977A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398215.3:c.467A>G MANE Select ENSP00000381273.2:p.Tyr156Cys
ENST00000651629.1:c.467A>G ENSP00000498905.1:p.Tyr156Cys
ENST00000398215.2:c.467A>G ENSP00000381273.2:p.Tyr156Cys
NM_000496.2:c.467A>G NP_000487.1:p.Tyr156Cys
XM_006724141.2:c.467A>G XP_006724204.1:p.Tyr156Cys
XM_011529900.1:c.467A>G XP_011528202.1:p.Tyr156Cys
XM_011529901.1:c.467A>G XP_011528203.1:p.Tyr156Cys
XM_006724141.3:c.467A>G XP_006724204.1:p.Tyr156Cys
XM_011529900.2:c.467A>G XP_011528202.1:p.Tyr156Cys
NM_000496.3:c.467A>G MANE Select NP_000487.1:p.Tyr156Cys