Canonical Allele Identifier: CA493124499
Gene: ABCA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2335503G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2285502G>A , CM000678.2:g.2285502G>A GRCh38
NC_000016.9:g.2335503G>A , CM000678.1:g.2335503G>A GRCh37
NC_000016.8:g.2275504G>A NCBI36
NG_011790.1:g.60245C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.3423C>T MANE Select ENSP00000301732.5:p.Phe1141=
ENST00000301732.9:c.3423C>T ENSP00000301732.5:p.Phe1141=
ENST00000382381.7:c.3249C>T ENSP00000371818.3:p.Phe1083=
NM_001089.2:c.3423C>T NP_001080.2:p.Phe1141=
NM_001089.3:c.3423C>T MANE Select NP_001080.2:p.Phe1141=
Search 100 bp 5'
Search 100 bp 3'