Canonical Allele Identifier: CA394353230
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs1379570761
gnomAD v2: 16-2376414-C-G
gnomAD v3: 16-2326413-C-G
gnomAD v4: 16-2326413-C-G
MyVariant Identifiers: chr16:g.2376414C>G (hg19) chr16:g.2326413C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326413C>G , CM000678.2:g.2326413C>G GRCh38
NC_000016.9:g.2376414C>G , CM000678.1:g.2376414C>G GRCh37
NC_000016.8:g.2316415C>G NCBI36
NG_011790.1:g.19334G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.54G>C MANE Select ENSP00000301732.5:p.Gln18His
ENST00000301732.9:c.54G>C ENSP00000301732.5:p.Gln18His
ENST00000382381.7:c.54G>C ENSP00000371818.3:p.Gln18His
ENST00000563623.5:n.617G>C
ENST00000567910.1:c.54G>C ENSP00000454397.1:p.Gln18His
NM_001089.2:c.54G>C NP_001080.2:p.Gln18His
NM_001089.3:c.54G>C MANE Select NP_001080.2:p.Gln18His
Search 100 bp 5'
Search 100 bp 3'