Canonical Allele Identifier: CA2631191248
Gene: ABCA3 HGNC NCBI

Linked Data

gnomAD v4: 16-2326372-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326372G>T , CM000678.2:g.2326372G>T GRCh38
NC_000016.9:g.2376373G>T , CM000678.1:g.2376373G>T GRCh37
NC_000016.8:g.2316374G>T NCBI36
NG_011790.1:g.19375C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.54+41C>A MANE Select ENSP00000301732.5:n.54+41C>A
ENST00000301732.9:c.54+41C>A ENSP00000301732.5:n.54+41C>A
ENST00000382381.7:c.54+41C>A ENSP00000371818.3:n.54+41C>A
ENST00000563623.5:n.617+41C>A
ENST00000567910.1:c.54+41C>A ENSP00000454397.1:n.54+41C>A
NM_001089.2:c.54+41C>A NP_001080.2:n.54+41C>A
NM_001089.3:c.54+41C>A MANE Select NP_001080.2:n.54+41C>A