Canonical Allele Identifier: CA719126285
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs1313879176
gnomAD v3: 16-2278259-T-A
gnomAD v4: 16-2278259-T-A
MyVariant Identifiers: chr16:g.2328260T>A (hg19) chr16:g.2278259T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278259T>A , CM000678.2:g.2278259T>A GRCh38
NC_000016.9:g.2328260T>A , CM000678.1:g.2328260T>A GRCh37
NC_000016.8:g.2268261T>A NCBI36
NG_011790.1:g.67488A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4718+29A>T MANE Select ENSP00000301732.5:n.4718+29A>T
ENST00000301732.9:c.4718+29A>T ENSP00000301732.5:n.4718+29A>T
ENST00000382381.7:c.4544+29A>T ENSP00000371818.3:n.4544+29A>T
NM_001089.2:c.4718+29A>T NP_001080.2:n.4718+29A>T
NM_001089.3:c.4718+29A>T MANE Select NP_001080.2:n.4718+29A>T
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