Canonical Allele Identifier: CA493093327
Gene: ABCA3 HGNC NCBI

Linked Data

gnomAD v4: 16-2278358-G-T
MyVariant Identifiers: chr16:g.2328359G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278358G>T , CM000678.2:g.2278358G>T GRCh38
NC_000016.9:g.2328359G>T , CM000678.1:g.2328359G>T GRCh37
NC_000016.8:g.2268360G>T NCBI36
NG_011790.1:g.67389C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.4648C>A MANE Select ENSP00000301732.5:p.Arg1550=
ENST00000301732.9:c.4648C>A ENSP00000301732.5:p.Arg1550=
ENST00000382381.7:c.4474C>A ENSP00000371818.3:p.Arg1492=
ENST00000566200.1:n.1169C>A
NM_001089.2:c.4648C>A NP_001080.2:p.Arg1550=
NM_001089.3:c.4648C>A MANE Select NP_001080.2:p.Arg1550=
Search 100 bp 5'
Search 100 bp 3'