Canonical Allele Identifier: CA427080731

Gene: SFTPB

Linked Data

• MyVariant Identifiers: chr2:g.85890601T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663478T>C , CM000664.2:g.85663478T>C	GRCh38
NC_000002.11:g.85890601T>C , CM000664.1:g.85890601T>C	GRCh37
NC_000002.10:g.85744112T>C	NCBI36
NG_016967.1:g.10264A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.870A>G	ENSP00000386346.2:p.Gly290=
ENST00000519937.7:c.870A>G MANE Select	ENSP00000428719.2:p.Gly290=
ENST00000393822.7:c.870A>G	ENSP00000377409.4:p.Gly290=
ENST00000409383.5:c.906A>G	ENSP00000386346.1:p.Gly302=
ENST00000428225.5:c.847A>G
ENST00000491167.1:n.70A>G
ENST00000494165.1:c.1A>G
ENST00000519937.6:c.870A>G	ENSP00000428719.2:p.Gly290=
NM_000542.3:c.906A>G	NP_000533.3:p.Gly302=
NM_198843.2:c.906A>G	NP_942140.2:p.Gly302=
XM_005264487.2:c.906A>G	XP_005264544.1:p.Gly302=
XM_005264488.2:c.858A>G	XP_005264545.2:p.Arg286=
XM_005264490.3:c.870A>G	XP_005264547.2:p.Gly290=
XM_005264488.4:c.858A>G	XP_005264545.2:p.Arg286=
XM_005264490.4:c.870A>G	XP_005264547.2:p.Gly290=
NM_000542.4:c.870A>G	NP_000533.4:p.Gly290=
NM_001367281.1:c.870A>G	NP_001354210.1:p.Gly290=
NM_198843.3:c.870A>G	NP_942140.3:p.Gly290=
NM_000542.5:c.870A>G MANE Select	NP_000533.4:p.Gly290=