Canonical Allele Identifier: CA719126292
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs1283777938
gnomAD v3: 16-2278261-C-G
gnomAD v4: 16-2278261-C-G
MyVariant Identifiers: chr16:g.2328262C>G (hg19) chr16:g.2278261C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278261C>G , CM000678.2:g.2278261C>G GRCh38
NC_000016.9:g.2328262C>G , CM000678.1:g.2328262C>G GRCh37
NC_000016.8:g.2268263C>G NCBI36
NG_011790.1:g.67486G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4718+27G>C MANE Select ENSP00000301732.5:n.4718+27G>C
ENST00000301732.9:c.4718+27G>C ENSP00000301732.5:n.4718+27G>C
ENST00000382381.7:c.4544+27G>C ENSP00000371818.3:n.4544+27G>C
NM_001089.2:c.4718+27G>C NP_001080.2:n.4718+27G>C
NM_001089.3:c.4718+27G>C MANE Select NP_001080.2:n.4718+27G>C
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