Canonical Allele Identifier: CA347487286

Gene: SFTPB

Linked Data

• MyVariant Identifiers: chr2:g.85890554G>C (hg19) ; chr2:g.85663431G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663431G>C , CM000664.2:g.85663431G>C	GRCh38
NC_000002.11:g.85890554G>C , CM000664.1:g.85890554G>C	GRCh37
NC_000002.10:g.85744065G>C	NCBI36
NG_016967.1:g.10311C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.917C>G	ENSP00000386346.2:p.Thr306Ser
ENST00000519937.7:c.917C>G MANE Select	ENSP00000428719.2:p.Thr306Ser
ENST00000393822.7:c.917C>G	ENSP00000377409.4:p.Thr306Ser
ENST00000409383.5:c.953C>G	ENSP00000386346.1:p.Thr318Ser
ENST00000428225.5:c.894C>G
ENST00000491167.1:n.117C>G
ENST00000494165.1:c.48C>G
ENST00000519937.6:c.917C>G	ENSP00000428719.2:p.Thr306Ser
NM_000542.3:c.953C>G	NP_000533.3:p.Thr318Ser
NM_198843.2:c.953C>G	NP_942140.2:p.Thr318Ser
XM_005264487.2:c.953C>G	XP_005264544.1:p.Thr318Ser
XM_005264488.2:c.905C>G	XP_005264545.2:p.Thr302Ser
XM_005264490.3:c.917C>G	XP_005264547.2:p.Thr306Ser
XM_005264488.4:c.905C>G	XP_005264545.2:p.Thr302Ser
XM_005264490.4:c.917C>G	XP_005264547.2:p.Thr306Ser
NM_000542.4:c.917C>G	NP_000533.4:p.Thr306Ser
NM_001367281.1:c.917C>G	NP_001354210.1:p.Thr306Ser
NM_198843.3:c.917C>G	NP_942140.3:p.Thr306Ser
NM_000542.5:c.917C>G MANE Select	NP_000533.4:p.Thr306Ser