Canonical Allele Identifier: CA427080617

Gene: SFTPB

Linked Data

• MyVariant Identifiers: chr2:g.85890517T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663394T>G , CM000664.2:g.85663394T>G	GRCh38
NC_000002.11:g.85890517T>G , CM000664.1:g.85890517T>G	GRCh37
NC_000002.10:g.85744028T>G	NCBI36
NG_016967.1:g.10348A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.954A>C	ENSP00000386346.2:p.Pro318=
ENST00000519937.7:c.954A>C MANE Select	ENSP00000428719.2:p.Pro318=
ENST00000393822.7:c.954A>C	ENSP00000377409.4:p.Pro318=
ENST00000409383.5:c.990A>C	ENSP00000386346.1:p.Pro330=
ENST00000428225.5:c.931A>C
ENST00000491167.1:n.154A>C
ENST00000494165.1:c.85A>C
ENST00000519937.6:c.954A>C	ENSP00000428719.2:p.Pro318=
NM_000542.3:c.990A>C	NP_000533.3:p.Pro330=
NM_198843.2:c.990A>C	NP_942140.2:p.Pro330=
XM_005264487.2:c.990A>C	XP_005264544.1:p.Pro330=
XM_005264488.2:c.942A>C	XP_005264545.2:p.Pro314=
XM_005264490.3:c.954A>C	XP_005264547.2:p.Pro318=
XM_005264488.4:c.942A>C	XP_005264545.2:p.Pro314=
XM_005264490.4:c.954A>C	XP_005264547.2:p.Pro318=
NM_000542.4:c.954A>C	NP_000533.4:p.Pro318=
NM_001367281.1:c.954A>C	NP_001354210.1:p.Pro318=
NM_198843.3:c.954A>C	NP_942140.3:p.Pro318=
NM_000542.5:c.954A>C MANE Select	NP_000533.4:p.Pro318=