Canonical Allele Identifier: CA493124586
Gene: ABCA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2335509G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2285508G>C , CM000678.2:g.2285508G>C GRCh38
NC_000016.9:g.2335509G>C , CM000678.1:g.2335509G>C GRCh37
NC_000016.8:g.2275510G>C NCBI36
NG_011790.1:g.60239C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.3417C>G MANE Select ENSP00000301732.5:p.Ala1139=
ENST00000301732.9:c.3417C>G ENSP00000301732.5:p.Ala1139=
ENST00000382381.7:c.3243C>G ENSP00000371818.3:p.Ala1081=
NM_001089.2:c.3417C>G NP_001080.2:p.Ala1139=
NM_001089.3:c.3417C>G MANE Select NP_001080.2:p.Ala1139=
Search 100 bp 5'
Search 100 bp 3'