Canonical Allele Identifier: CA620708156
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs535607538
gnomAD v2: 16-2327842-G-A
gnomAD v4: 16-2277841-G-A
MyVariant Identifiers: chr16:g.2327842G>A (hg19) chr16:g.2277841G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2277841G>A , CM000678.2:g.2277841G>A GRCh38
NC_000016.9:g.2327842G>A , CM000678.1:g.2327842G>A GRCh37
NC_000016.8:g.2267843G>A NCBI36
NG_011790.1:g.67906C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.4909+38C>T MANE Select ENSP00000301732.5:n.4909+38C>T
ENST00000301732.9:c.4909+38C>T ENSP00000301732.5:n.4909+38C>T
ENST00000382381.7:c.4735+38C>T ENSP00000371818.3:n.4735+38C>T
NM_001089.2:c.4909+38C>T NP_001080.2:n.4909+38C>T
NM_001089.3:c.4909+38C>T MANE Select NP_001080.2:n.4909+38C>T
Search 100 bp 5'
Search 100 bp 3'