Canonical Allele Identifier: CA347487101

Gene: SFTPB

Linked Data

• gnomAD v4: 2-85663387-T-C
• MyVariant Identifiers: chr2:g.85890510T>C (hg19) ; chr2:g.85663387T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663387T>C , CM000664.2:g.85663387T>C	GRCh38
NC_000002.11:g.85890510T>C , CM000664.1:g.85890510T>C	GRCh37
NC_000002.10:g.85744021T>C	NCBI36
NG_016967.1:g.10355A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.961A>G	ENSP00000386346.2:p.Met321Val
ENST00000519937.7:c.961A>G MANE Select	ENSP00000428719.2:p.Met321Val
ENST00000393822.7:c.961A>G	ENSP00000377409.4:p.Met321Val
ENST00000409383.5:c.997A>G	ENSP00000386346.1:p.Met333Val
ENST00000428225.5:c.938A>G
ENST00000491167.1:n.161A>G
ENST00000494165.1:c.92A>G
ENST00000519937.6:c.961A>G	ENSP00000428719.2:p.Met321Val
NM_000542.3:c.997A>G	NP_000533.3:p.Met333Val
NM_198843.2:c.997A>G	NP_942140.2:p.Met333Val
XM_005264487.2:c.997A>G	XP_005264544.1:p.Met333Val
XM_005264488.2:c.949A>G	XP_005264545.2:p.Met317Val
XM_005264490.3:c.961A>G	XP_005264547.2:p.Met321Val
XM_005264488.4:c.949A>G	XP_005264545.2:p.Met317Val
XM_005264490.4:c.961A>G	XP_005264547.2:p.Met321Val
NM_000542.4:c.961A>G	NP_000533.4:p.Met321Val
NM_001367281.1:c.961A>G	NP_001354210.1:p.Met321Val
NM_198843.3:c.961A>G	NP_942140.3:p.Met321Val
NM_000542.5:c.961A>G MANE Select	NP_000533.4:p.Met321Val