Canonical Allele Identifier: CA493167441
Gene: ABCA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2367754G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2317753G>C , CM000678.2:g.2317753G>C GRCh38
NC_000016.9:g.2367754G>C , CM000678.1:g.2367754G>C GRCh37
NC_000016.8:g.2307755G>C NCBI36
NG_011790.1:g.27994C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.885C>G MANE Select ENSP00000301732.5:p.Arg295=
ENST00000301732.9:c.885C>G ENSP00000301732.5:p.Arg295=
ENST00000382381.7:c.885C>G ENSP00000371818.3:p.Arg295=
ENST00000563623.5:n.1448C>G
NM_001089.2:c.885C>G NP_001080.2:p.Arg295=
NM_001089.3:c.885C>G MANE Select NP_001080.2:p.Arg295=