Canonical Allele Identifier: CA394305508
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs2093649740
gnomAD v3: 16-2278309-G-A
gnomAD v4: 16-2278309-G-A
MyVariant Identifiers: chr16:g.2328310G>A (hg19) chr16:g.2278309G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278309G>A , CM000678.2:g.2278309G>A GRCh38
NC_000016.9:g.2328310G>A , CM000678.1:g.2328310G>A GRCh37
NC_000016.8:g.2268311G>A NCBI36
NG_011790.1:g.67438C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4697C>T MANE Select ENSP00000301732.5:p.Ala1566Val
ENST00000301732.9:c.4697C>T ENSP00000301732.5:p.Ala1566Val
ENST00000382381.7:c.4523C>T ENSP00000371818.3:p.Ala1508Val
ENST00000566200.1:n.1218C>T
NM_001089.2:c.4697C>T NP_001080.2:p.Ala1566Val
NM_001089.3:c.4697C>T MANE Select NP_001080.2:p.Ala1566Val
Search 100 bp 5'
Search 100 bp 3'