Canonical Allele Identifier: CA276819439
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs962155748
gnomAD v3: 16-2276629-C-A
gnomAD v4: 16-2276629-C-A
MyVariant Identifiers: chr16:g.2326630C>A (hg19) chr16:g.2276629C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2276629C>A , CM000678.2:g.2276629C>A GRCh38
NC_000016.9:g.2326630C>A , CM000678.1:g.2326630C>A GRCh37
NC_000016.8:g.2266631C>A NCBI36
NG_011790.1:g.69118G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.*45G>T MANE Select ENSP00000301732.5:n.*45G>T
ENST00000301732.9:c.*45G>T ENSP00000301732.5:n.*45G>T
ENST00000382381.7:c.*45G>T ENSP00000371818.3:n.*45G>T
NM_001089.2:c.*45G>T NP_001080.2:n.*45G>T
NM_001089.3:c.*45G>T MANE Select NP_001080.2:n.*45G>T
Search 100 bp 5'
Search 100 bp 3'