Canonical Allele Identifier: CA493092821
Gene: ABCA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2328330T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278329T>C , CM000678.2:g.2278329T>C GRCh38
NC_000016.9:g.2328330T>C , CM000678.1:g.2328330T>C GRCh37
NC_000016.8:g.2268331T>C NCBI36
NG_011790.1:g.67418A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4677A>G MANE Select ENSP00000301732.5:p.Arg1559=
ENST00000301732.9:c.4677A>G ENSP00000301732.5:p.Arg1559=
ENST00000382381.7:c.4503A>G ENSP00000371818.3:p.Arg1501=
ENST00000566200.1:n.1198A>G
NM_001089.2:c.4677A>G NP_001080.2:p.Arg1559=
NM_001089.3:c.4677A>G MANE Select NP_001080.2:p.Arg1559=