Canonical Allele Identifier: CA1266876863

Gene: SFTPB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663319A= , CM000664.2:g.85663319A=	GRCh38
NC_000002.11:g.85890442A= , CM000664.1:g.85890442A=	GRCh37
NC_000002.10:g.85743953A=	NCBI36
NG_016967.1:g.10423T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.1002+27T=	ENSP00000386346.2:n.1002+27T=
ENST00000519937.7:c.1002+27T= MANE Select	ENSP00000428719.2:n.1002+27T=
ENST00000393822.7:c.1002+27T=	ENSP00000377409.4:n.1002+27T=
ENST00000409383.5:c.1038+27T=	ENSP00000386346.1:n.1038+27T=
ENST00000428225.5:c.979+27T=
ENST00000491167.1:n.202+27T=
ENST00000494165.1:c.133+27T=
ENST00000519937.6:c.1002+27T=	ENSP00000428719.2:n.1002+27T=
NM_000542.3:c.1038+27T=	NP_000533.3:n.1038+27T=
NM_198843.2:c.1038+27T=	NP_942140.2:n.1038+27T=
XM_005264487.2:c.1038+27T=	XP_005264544.1:n.1038+27T=
XM_005264488.2:c.990+27T=	XP_005264545.2:n.990+27T=
XM_005264490.3:c.1002+27T=	XP_005264547.2:n.1002+27T=
XM_005264488.4:c.990+27T=	XP_005264545.2:n.990+27T=
XM_005264490.4:c.1002+27T=	XP_005264547.2:n.1002+27T=
NM_000542.4:c.1002+27T=	NP_000533.4:n.1002+27T=
NM_001367281.1:c.1002+27T=	NP_001354210.1:n.1002+27T=
NM_198843.3:c.1002+27T=	NP_942140.3:n.1002+27T=
NM_000542.5:c.1002+27T= MANE Select	NP_000533.4:n.1002+27T=