Canonical Allele Identifier: CA394305438
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs1596827048
MyVariant Identifiers: chr16:g.2328299T>G (hg19) chr16:g.2278298T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278298T>G , CM000678.2:g.2278298T>G GRCh38
NC_000016.9:g.2328299T>G , CM000678.1:g.2328299T>G GRCh37
NC_000016.8:g.2268300T>G NCBI36
NG_011790.1:g.67449A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4708A>C MANE Select ENSP00000301732.5:p.Thr1570Pro
ENST00000301732.9:c.4708A>C ENSP00000301732.5:p.Thr1570Pro
ENST00000382381.7:c.4534A>C ENSP00000371818.3:p.Thr1512Pro
ENST00000566200.1:n.1229A>C
NM_001089.2:c.4708A>C NP_001080.2:p.Thr1570Pro
NM_001089.3:c.4708A>C MANE Select NP_001080.2:p.Thr1570Pro
Search 100 bp 5'
Search 100 bp 3'