Canonical Allele Identifier: CA394304514
Gene: ABCA3 HGNC NCBI

Linked Data

gnomAD v4: 16-2277938-C-T
MyVariant Identifiers: chr16:g.2327939C>T (hg19) chr16:g.2277938C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2277938C>T , CM000678.2:g.2277938C>T GRCh38
NC_000016.9:g.2327939C>T , CM000678.1:g.2327939C>T GRCh37
NC_000016.8:g.2267940C>T NCBI36
NG_011790.1:g.67809G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4850G>A MANE Select ENSP00000301732.5:p.Ser1617Asn
ENST00000301732.9:c.4850G>A ENSP00000301732.5:p.Ser1617Asn
ENST00000382381.7:c.4676G>A ENSP00000371818.3:p.Ser1559Asn
NM_001089.2:c.4850G>A NP_001080.2:p.Ser1617Asn
NM_001089.3:c.4850G>A MANE Select NP_001080.2:p.Ser1617Asn
Search 100 bp 5'
Search 100 bp 3'