Canonical Allele Identifier: CA620390510
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs929760139
gnomAD v2: 16-2367570-A-T
gnomAD v3: 16-2317569-A-T
gnomAD v4: 16-2317569-A-T
MyVariant Identifiers: chr16:g.2367570A>T (hg19) chr16:g.2317569A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2317569A>T , CM000678.2:g.2317569A>T GRCh38
NC_000016.9:g.2367570A>T , CM000678.1:g.2367570A>T GRCh37
NC_000016.8:g.2307571A>T NCBI36
NG_011790.1:g.28178T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.990+79T>A MANE Select ENSP00000301732.5:n.990+79T>A
ENST00000301732.9:c.990+79T>A ENSP00000301732.5:n.990+79T>A
ENST00000382381.7:c.990+79T>A ENSP00000371818.3:n.990+79T>A
ENST00000563623.5:n.1553+79T>A
NM_001089.2:c.990+79T>A NP_001080.2:n.990+79T>A
NM_001089.3:c.990+79T>A MANE Select NP_001080.2:n.990+79T>A
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