Canonical Allele Identifier: CA276820630
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs532913711
gnomAD v3: 16-2278141-C-T
gnomAD v4: 16-2278141-C-T
MyVariant Identifiers: chr16:g.2328142C>T (hg19) chr16:g.2278141C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278141C>T , CM000678.2:g.2278141C>T GRCh38
NC_000016.9:g.2328142C>T , CM000678.1:g.2328142C>T GRCh37
NC_000016.8:g.2268143C>T NCBI36
NG_011790.1:g.67606G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4719-72G>A MANE Select ENSP00000301732.5:n.4719-72G>A
ENST00000301732.9:c.4719-72G>A ENSP00000301732.5:n.4719-72G>A
ENST00000382381.7:c.4545-72G>A ENSP00000371818.3:n.4545-72G>A
NM_001089.2:c.4719-72G>A NP_001080.2:n.4719-72G>A
NM_001089.3:c.4719-72G>A MANE Select NP_001080.2:n.4719-72G>A
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