Canonical Allele Identifier: CA7841825
Gene: ABCA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2776734
ClinVar RCV Id: RCV003664885
dbSNP Id: rs747304976
ExAC: 16:2376444 C / T
gnomAD v2: 16-2376444-C-T
gnomAD v3: 16-2326443-C-T
gnomAD v4: 16-2326443-C-T
MyVariant Identifiers: chr16:g.2376444C>T (hg19) chr16:g.2326443C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326443C>T , CM000678.2:g.2326443C>T GRCh38
NC_000016.9:g.2376444C>T , CM000678.1:g.2376444C>T GRCh37
NC_000016.8:g.2316445C>T NCBI36
NG_011790.1:g.19304G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.24G>A MANE Select ENSP00000301732.5:p.Ala8=
ENST00000301732.9:c.24G>A ENSP00000301732.5:p.Ala8=
ENST00000382381.7:c.24G>A ENSP00000371818.3:p.Ala8=
ENST00000563623.5:n.587G>A
ENST00000567910.1:c.24G>A ENSP00000454397.1:p.Ala8=
NM_001089.2:c.24G>A NP_001080.2:p.Ala8=
NM_001089.3:c.24G>A MANE Select NP_001080.2:p.Ala8=
Search 100 bp 5'
Search 100 bp 3'