Canonical Allele Identifier: CA1743860
Gene: SFTPB HGNC NCBI

Linked Data

dbSNP Id: rs777177263
gnomAD v2: 2-85890549-G-A
gnomAD v4: 2-85663426-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85663426G>A , CM000664.2:g.85663426G>A GRCh38
NC_000002.11:g.85890549G>A , CM000664.1:g.85890549G>A GRCh37
NC_000002.10:g.85744060G>A NCBI36
NG_016967.1:g.10316C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409383.6:c.922C>T ENSP00000386346.2:p.Gln308Ter
ENST00000519937.7:c.922C>T MANE Select ENSP00000428719.2:p.Gln308Ter
ENST00000393822.7:c.922C>T ENSP00000377409.4:p.Gln308Ter
ENST00000409383.5:c.958C>T ENSP00000386346.1:p.Gln320Ter
ENST00000428225.5:c.899C>T
ENST00000491167.1:n.122C>T
ENST00000494165.1:c.53C>T
ENST00000519937.6:c.922C>T ENSP00000428719.2:p.Gln308Ter
NM_000542.3:c.958C>T NP_000533.3:p.Gln320Ter
NM_198843.2:c.958C>T NP_942140.2:p.Gln320Ter
XM_005264487.2:c.958C>T XP_005264544.1:p.Gln320Ter
XM_005264488.2:c.910C>T XP_005264545.2:p.Gln304Ter
XM_005264490.3:c.922C>T XP_005264547.2:p.Gln308Ter
XM_005264488.4:c.910C>T XP_005264545.2:p.Gln304Ter
XM_005264490.4:c.922C>T XP_005264547.2:p.Gln308Ter
NM_000542.4:c.922C>T NP_000533.4:p.Gln308Ter
NM_001367281.1:c.922C>T NP_001354210.1:p.Gln308Ter
NM_198843.3:c.922C>T NP_942140.3:p.Gln308Ter
NM_000542.5:c.922C>T MANE Select NP_000533.4:p.Gln308Ter