Canonical Allele Identifier: CA347487574

Gene: SFTPB

Linked Data

• MyVariant Identifiers: chr2:g.85890603C>G (hg19) ; chr2:g.85663480C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663480C>G , CM000664.2:g.85663480C>G	GRCh38
NC_000002.11:g.85890603C>G , CM000664.1:g.85890603C>G	GRCh37
NC_000002.10:g.85744114C>G	NCBI36
NG_016967.1:g.10262G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.868G>C	ENSP00000386346.2:p.Gly290Arg
ENST00000519937.7:c.868G>C MANE Select	ENSP00000428719.2:p.Gly290Arg
ENST00000393822.7:c.868G>C	ENSP00000377409.4:p.Gly290Arg
ENST00000409383.5:c.904G>C	ENSP00000386346.1:p.Gly302Arg
ENST00000428225.5:c.846-1G>C
ENST00000491167.1:n.68G>C
ENST00000519937.6:c.868G>C	ENSP00000428719.2:p.Gly290Arg
NM_000542.3:c.904G>C	NP_000533.3:p.Gly302Arg
NM_198843.2:c.904G>C	NP_942140.2:p.Gly302Arg
XM_005264487.2:c.904G>C	XP_005264544.1:p.Gly302Arg
XM_005264488.2:c.857-1G>C	XP_005264545.2:n.857-1G>C
XM_005264490.3:c.868G>C	XP_005264547.2:p.Gly290Arg
XM_005264488.4:c.857-1G>C	XP_005264545.2:n.857-1G>C
XM_005264490.4:c.868G>C	XP_005264547.2:p.Gly290Arg
NM_000542.4:c.868G>C	NP_000533.4:p.Gly290Arg
NM_001367281.1:c.868G>C	NP_001354210.1:p.Gly290Arg
NM_198843.3:c.868G>C	NP_942140.3:p.Gly290Arg
NM_000542.5:c.868G>C MANE Select	NP_000533.4:p.Gly290Arg