Canonical Allele Identifier: CA493093387
Gene: ABCA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2328363C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278362C>G , CM000678.2:g.2278362C>G GRCh38
NC_000016.9:g.2328363C>G , CM000678.1:g.2328363C>G GRCh37
NC_000016.8:g.2268364C>G NCBI36
NG_011790.1:g.67385G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4644G>C MANE Select ENSP00000301732.5:p.Val1548=
ENST00000301732.9:c.4644G>C ENSP00000301732.5:p.Val1548=
ENST00000382381.7:c.4470G>C ENSP00000371818.3:p.Val1490=
ENST00000566200.1:n.1165G>C
NM_001089.2:c.4644G>C NP_001080.2:p.Val1548=
NM_001089.3:c.4644G>C MANE Select NP_001080.2:p.Val1548=