Canonical Allele Identifier: CA493361448
Gene: ABCA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2376021G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326020G>A , CM000678.2:g.2326020G>A GRCh38
NC_000016.9:g.2376021G>A , CM000678.1:g.2376021G>A GRCh37
NC_000016.8:g.2316022G>A NCBI36
NG_011790.1:g.19727C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.309C>T MANE Select ENSP00000301732.5:p.Ile103=
ENST00000301732.9:c.309C>T ENSP00000301732.5:p.Ile103=
ENST00000382381.7:c.309C>T ENSP00000371818.3:p.Ile103=
ENST00000563623.5:n.872C>T
ENST00000567910.1:c.309C>T ENSP00000454397.1:p.Ile103=
NM_001089.2:c.309C>T NP_001080.2:p.Ile103=
NM_001089.3:c.309C>T MANE Select NP_001080.2:p.Ile103=