Canonical Allele Identifier: CA11021249
Gene: CRACDL HGNC NCBI

Linked Data

dbSNP Id: rs6733011
gnomAD v2: 2-99465502-A-G
gnomAD v3: 2-98849039-A-G
gnomAD v4: 2-98849039-A-G
MyVariant Identifiers: chr2:g.99465502A>G (hg19) chr2:g.98849039A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.98849039A>G , CM000664.2:g.98849039A>G GRCh38
NC_000002.11:g.99465502A>G , CM000664.1:g.99465502A>G GRCh37
NC_000002.10:g.98831934A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000397899.7:c.-10-2229T>C MANE Select ENSP00000380996.2:n.-10-2229T>C
ENST00000397899.6:c.-10-2229T>C ENSP00000380996.2:n.-10-2229T>C
ENST00000415261.5:c.33-2229T>C ENSP00000390799.1:n.33-2229T>C
ENST00000420294.1:c.33-2229T>C ENSP00000403428.1:n.33-2229T>C
ENST00000423771.5:c.75-2229T>C ENSP00000396657.1:n.75-2229T>C
ENST00000428096.5:c.33-2229T>C ENSP00000387902.1:n.33-2229T>C
ENST00000462314.1:n.238-2229T>C
ENST00000612523.4:c.-28-2229T>C ENSP00000480530.1:n.-28-2229T>C
NM_207362.2:c.-10-2229T>C NP_997245.2:n.-10-2229T>C
XM_005263923.2:c.75-2229T>C XP_005263980.1:n.75-2229T>C
XM_005263924.2:c.75-2229T>C XP_005263981.1:n.75-2229T>C
XM_005263926.2:c.-10-2229T>C XP_005263983.1:n.-10-2229T>C
XM_011511093.1:c.33-2229T>C XP_011509395.1:n.33-2229T>C
XM_011511094.1:c.-10-2229T>C XP_011509396.1:n.-10-2229T>C
XM_011511095.1:c.-10-2229T>C XP_011509397.1:n.-10-2229T>C
XM_005263923.3:c.75-2229T>C XP_005263980.1:n.75-2229T>C
XM_005263924.3:c.75-2229T>C XP_005263981.1:n.75-2229T>C
XM_005263926.3:c.-10-2229T>C XP_005263983.1:n.-10-2229T>C
XM_011511095.2:c.-10-2229T>C XP_011509397.1:n.-10-2229T>C
XM_017003971.1:c.33-2229T>C XP_016859460.1:n.33-2229T>C
XM_017003972.1:c.33-2229T>C XP_016859461.1:n.33-2229T>C
XM_017003973.1:c.75-2229T>C XP_016859462.1:n.75-2229T>C
NM_207362.3:c.-10-2229T>C MANE Select NP_997245.2:n.-10-2229T>C
Search 100 bp 5'
Search 100 bp 3'