Canonical Allele Identifier: CA347486912
Gene: SFTPB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85663348T>G , CM000664.2:g.85663348T>G GRCh38
NC_000002.11:g.85890471T>G , CM000664.1:g.85890471T>G GRCh37
NC_000002.10:g.85743982T>G NCBI36
NG_016967.1:g.10394A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409383.6:c.1000A>C ENSP00000386346.2:p.Lys334Gln
ENST00000519937.7:c.1000A>C MANE Select ENSP00000428719.2:p.Lys334Gln
ENST00000393822.7:c.1000A>C ENSP00000377409.4:p.Lys334Gln
ENST00000409383.5:c.1036A>C ENSP00000386346.1:p.Lys346Gln
ENST00000428225.5:c.977A>C
ENST00000491167.1:n.200A>C
ENST00000494165.1:c.131A>C
ENST00000519937.6:c.1000A>C ENSP00000428719.2:p.Lys334Gln
NM_000542.3:c.1036A>C NP_000533.3:p.Lys346Gln
NM_198843.2:c.1036A>C NP_942140.2:p.Lys346Gln
XM_005264487.2:c.1036A>C XP_005264544.1:p.Lys346Gln
XM_005264488.2:c.988A>C XP_005264545.2:p.Lys330Gln
XM_005264490.3:c.1000A>C XP_005264547.2:p.Lys334Gln
XM_005264488.4:c.988A>C XP_005264545.2:p.Lys330Gln
XM_005264490.4:c.1000A>C XP_005264547.2:p.Lys334Gln
NM_000542.4:c.1000A>C NP_000533.4:p.Lys334Gln
NM_001367281.1:c.1000A>C NP_001354210.1:p.Lys334Gln
NM_198843.3:c.1000A>C NP_942140.3:p.Lys334Gln
NM_000542.5:c.1000A>C MANE Select NP_000533.4:p.Lys334Gln