Canonical Allele Identifier: CA114626
Gene: CA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 919
ClinVar RCV Id: RCV000000967
dbSNP Id: rs118203934

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.85465357T>G , CM000670.2:g.85465357T>G GRCh38
NC_000008.10:g.86377586T>G , CM000670.1:g.86377586T>G GRCh37
NC_000008.9:g.86564838T>G NCBI36
NG_007287.1:g.6341T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000285379.10:c.120T>G MANE Select ENSP00000285379.4:p.Tyr40Ter
ENST00000285379.9:c.120T>G ENSP00000285379.4:p.Tyr40Ter
ENST00000518231.1:n.191T>G
ENST00000520127.5:c.120T>G ENSP00000428443.1:p.Tyr40Ter
ENST00000520996.5:n.199T>G
ENST00000522742.1:c.120T>G ENSP00000428947.1:p.Tyr40Ter
NM_000067.2:c.120T>G NP_000058.1:p.Tyr40Ter
NM_001293675.1:c.-65T>G NP_001280604.1:n.-65T>G
NM_000067.3:c.120T>G MANE Select NP_000058.1:p.Tyr40Ter
NM_001293675.2:c.-65T>G NP_001280604.1:n.-65T>G