Canonical Allele Identifier: CA276825493
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs1028268838
gnomAD v3: 16-2289462-T-C
gnomAD v4: 16-2289462-T-C
MyVariant Identifiers: chr16:g.2339463T>C (hg19) chr16:g.2289462T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2289462T>C , CM000678.2:g.2289462T>C GRCh38
NC_000016.9:g.2339463T>C , CM000678.1:g.2339463T>C GRCh37
NC_000016.8:g.2279464T>C NCBI36
NG_011790.1:g.56285A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.2672A>G MANE Select ENSP00000301732.5:p.Glu891Gly
ENST00000301732.9:c.2672A>G ENSP00000301732.5:p.Glu891Gly
ENST00000382381.7:c.2498A>G ENSP00000371818.3:p.Glu833Gly
ENST00000563623.5:n.3235A>G
NM_001089.2:c.2672A>G NP_001080.2:p.Glu891Gly
NM_001089.3:c.2672A>G MANE Select NP_001080.2:p.Glu891Gly
Search 100 bp 5'
Search 100 bp 3'