Canonical Allele Identifier: CA18979850
Gene: CDA HGNC NCBI

Linked Data

dbSNP Id: rs899577927
gnomAD v3: 1-20618383-T-G
gnomAD v4: 1-20618383-T-G
MyVariant Identifiers: chr1:g.20944876T>G (hg19) chr1:g.20618383T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618383T>G , CM000663.2:g.20618383T>G GRCh38
NC_000001.10:g.20944876T>G , CM000663.1:g.20944876T>G GRCh37
NC_000001.9:g.20817463T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-69T>G MANE Select ENSP00000364212.3:n.325-69T>G
ENST00000375071.3:c.325-69T>G ENSP00000364212.3:n.325-69T>G
ENST00000461985.1:n.311-69T>G
NM_001785.2:c.325-69T>G NP_001776.1:n.325-69T>G
NM_001785.3:c.325-69T>G MANE Select NP_001776.1:n.325-69T>G
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