Canonical Allele Identifier: CA607360481
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs1302902148
gnomAD v2: 12-112244363-G-C
gnomAD v3: 12-111806559-G-C
gnomAD v4: 12-111806559-G-C
MyVariant Identifiers: chr12:g.112244363G>C (hg19) chr12:g.111806559G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111806559G>C , CM000674.2:g.111806559G>C GRCh38
NC_000012.11:g.112244363G>C , CM000674.1:g.112244363G>C GRCh37
NC_000012.10:g.110728746G>C NCBI36
NG_012250.1:g.45018G>C
NG_012250.2:g.44673G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.1521+2586G>C MANE Select ENSP00000261733.2:n.1521+2586G>C
ENST00000261733.6:c.1521+2586G>C ENSP00000261733.2:n.1521+2586G>C
ENST00000416293.7:c.1380+2586G>C ENSP00000403349.3:n.1380+2586G>C
ENST00000548536.1:c.*1397+2586G>C ENSP00000448179.1:n.*1397+2586G>C
ENST00000549106.1:c.452+2586G>C
NM_000690.3:c.1521+2586G>C NP_000681.2:n.1521+2586G>C
NM_001204889.1:c.1380+2586G>C NP_001191818.1:n.1380+2586G>C
NM_000690.4:c.1521+2586G>C MANE Select NP_000681.2:n.1521+2586G>C
NM_001204889.2:c.1380+2586G>C NP_001191818.1:n.1380+2586G>C
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