Canonical Allele Identifier: CA973785778
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs2093685887
gnomAD v3: 16-2299671-T-C
gnomAD v4: 16-2299671-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2299671T>C , CM000678.2:g.2299671T>C GRCh38
NC_000016.9:g.2349672T>C , CM000678.1:g.2349672T>C GRCh37
NC_000016.8:g.2289673T>C NCBI36
NG_011790.1:g.46076A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.1612-139A>G MANE Select ENSP00000301732.5:n.1612-139A>G
ENST00000301732.9:c.1612-139A>G ENSP00000301732.5:n.1612-139A>G
ENST00000382381.7:c.1438-139A>G ENSP00000371818.3:n.1438-139A>G
ENST00000563623.5:n.2175-139A>G
NM_001089.2:c.1612-139A>G NP_001080.2:n.1612-139A>G
NM_001089.3:c.1612-139A>G MANE Select NP_001080.2:n.1612-139A>G