Canonical Allele Identifier: CA1266879685
Gene: SFTPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85668581C= , CM000664.2:g.85668581C= GRCh38
NC_000002.11:g.85895704C= , CM000664.1:g.85895704C= GRCh37
NC_000002.10:g.85749215C= NCBI36
NG_016967.1:g.5161G=

Transcript Alleles

HGVS Amino-acid Change
NM_000542.3:c.-33+93G= NP_000533.3:n.-33+93G=
NM_198843.2:c.-33+93G= NP_942140.2:n.-33+93G=
NM_198843.3:c.-69+93G= NP_942140.3:n.-69+93G=
ENST00000393822.7:c.-69+93G= ENSP00000377409.4:n.-69+93G=
ENST00000409383.5:c.-33+93G= ENSP00000386346.1:n.-33+93G=
ENST00000409383.6:c.-69+93G= ENSP00000386346.2:n.-69+93G=