Canonical Allele Identifier: CA394305901
Gene: ABCA3 HGNC NCBI

Linked Data

gnomAD v4: 16-2278375-C-G
MyVariant Identifiers: chr16:g.2328376C>G (hg19) chr16:g.2278375C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278375C>G , CM000678.2:g.2278375C>G GRCh38
NC_000016.9:g.2328376C>G , CM000678.1:g.2328376C>G GRCh37
NC_000016.8:g.2268377C>G NCBI36
NG_011790.1:g.67372G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4631G>C MANE Select ENSP00000301732.5:p.Gly1544Ala
ENST00000301732.9:c.4631G>C ENSP00000301732.5:p.Gly1544Ala
ENST00000382381.7:c.4457G>C ENSP00000371818.3:p.Gly1486Ala
ENST00000566200.1:n.1152G>C
NM_001089.2:c.4631G>C NP_001080.2:p.Gly1544Ala
NM_001089.3:c.4631G>C MANE Select NP_001080.2:p.Gly1544Ala
Search 100 bp 5'
Search 100 bp 3'