Canonical Allele Identifier: CA228547071

Linked Data

dbSNP Id: rs2234702

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111912374G>A , CM000673.2:g.111912374G>A GRCh38
NC_000011.9:g.111783098G>A , CM000673.1:g.111783098G>A GRCh37
NC_000011.8:g.111288308G>A NCBI36
NG_009824.2:g.16349C>T
NG_033080.1:g.4639G>A
NG_009824.3:g.16349C>T
NG_033080.2:g.4639G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000526180.6:c.-224-426C>T (CRYAB) ENSP00000436051.1:n.-224-426C>T
ENST00000527899.6:c.-198-452C>T (CRYAB) ENSP00000436089.2:n.-198-452C>T
ENST00000533475.6:c.-198-452C>T (CRYAB) ENSP00000433560.1:n.-198-452C>T
ENST00000533879.2:c.-198-452C>T (CRYAB) ENSP00000435931.2:n.-198-452C>T
ENST00000533971.2:c.-198-452C>T (CRYAB) ENSP00000434269.1:n.-198-452C>T
ENST00000616970.5:c.-198-452C>T (CRYAB) ENSP00000483554.1:n.-198-452C>T
ENST00000652223.1:n.115-452C>T (CRYAB)
ENST00000652606.1:n.47-452C>T (CRYAB)
ENST00000304298.3:c.-456G>A (HSPB2) ENSP00000302476.3:n.-456G>A
ENST00000527899.5:c.-198-452C>T (CRYAB) ENSP00000436089.1:n.-198-452C>T
ENST00000527950.5:c.-198-452C>T (CRYAB) ENSP00000437149.1:n.-198-452C>T
ENST00000528628.5:c.-199+360C>T (CRYAB) ENSP00000432182.1:n.-199+360C>T
ENST00000529647.5:c.-198-452C>T (CRYAB) ENSP00000431754.1:n.-198-452C>T
ENST00000531198.5:c.-274-36C>T (CRYAB) ENSP00000434247.1:n.-274-36C>T
ENST00000533475.5:c.-198-452C>T (CRYAB) ENSP00000433560.1:n.-198-452C>T
ENST00000533879.1:c.-198-452C>T (CRYAB) ENSP00000435931.1:n.-198-452C>T
ENST00000616970.4:c.-198-452C>T (CRYAB) ENSP00000483554.1:n.-198-452C>T
NM_001289807.1:c.-198-452C>T (CRYAB) NP_001276736.1:n.-198-452C>T
NM_001885.2:c.-198-452C>T (CRYAB) NP_001876.1:n.-198-452C>T
XM_011542608.1:c.-199+360C>T (CRYAB) XP_011540910.1:n.-199+360C>T
NM_001368245.1:c.-198-452C>T (CRYAB) NP_001355174.1:n.-198-452C>T
NM_001885.3:c.-198-452C>T (CRYAB) NP_001876.1:n.-198-452C>T