Canonical Allele Identifier: CA2012830660
Community Standard Title: NM_001144958.2(CRACR2A):c.-36-8037C=
Gene: CRACR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3705072G= , CM000674.2:g.3705072G= GRCh38
NC_000012.11:g.3814238G= , CM000674.1:g.3814238G= GRCh37
NC_000012.10:g.3684499G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001144958.2:c.-36-8037C= MANE Select NP_001138430.1:n.-36-8037C=
ENST00000440314.7:c.-36-8037C= MANE Select ENSP00000409382.2:n.-36-8037C=
NM_001144958.1:c.-36-8037C= NP_001138430.1:n.-36-8037C=
NM_032680.3:c.-36-8037C= NP_116069.1:n.-36-8037C=
NM_032680.4:c.-36-8037C= NP_116069.1:n.-36-8037C=
ENST00000252322.1:c.-36-8037C= ENSP00000252322.1:n.-36-8037C=
ENST00000440314.6:c.-36-8037C= ENSP00000409382.2:n.-36-8037C=
XM_006719021.2:c.-36-8037C= XP_006719084.1:n.-36-8037C=
XM_006719021.3:c.-36-8037C= XP_006719084.1:n.-36-8037C=
XM_011521034.1:c.-36-8037C= XP_011519336.1:n.-36-8037C=
XM_011521034.3:c.-36-8037C= XP_011519336.1:n.-36-8037C=
XM_011521035.1:c.-36-8037C= XP_011519337.1:n.-36-8037C=