Canonical Allele Identifier: CA493093006
Gene: ABCA3 HGNC NCBI

Linked Data

gnomAD v4: 16-2278338-G-T
MyVariant Identifiers: chr16:g.2328339G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278338G>T , CM000678.2:g.2278338G>T GRCh38
NC_000016.9:g.2328339G>T , CM000678.1:g.2328339G>T GRCh37
NC_000016.8:g.2268340G>T NCBI36
NG_011790.1:g.67409C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4668C>A MANE Select ENSP00000301732.5:p.Thr1556=
ENST00000301732.9:c.4668C>A ENSP00000301732.5:p.Thr1556=
ENST00000382381.7:c.4494C>A ENSP00000371818.3:p.Thr1498=
ENST00000566200.1:n.1189C>A
NM_001089.2:c.4668C>A NP_001080.2:p.Thr1556=
NM_001089.3:c.4668C>A MANE Select NP_001080.2:p.Thr1556=