Canonical Allele Identifier: CA377352791

Gene: SFTPA2

Linked Data

• dbSNP Id: rs1168257966
• gnomAD v2: 10-81317059-C-A
• gnomAD v4: 10-79557303-C-A
• MyVariant Identifiers: chr10:g.81317059C>A (hg19) ; chr10:g.79557303C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79557303C>A , CM000672.2:g.79557303C>A	GRCh38
NC_000010.10:g.81317059C>A , CM000672.1:g.81317059C>A	GRCh37
NG_013046.1:g.8105G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.653G>T MANE Select	ENSP00000361400.2:p.Gly218Val
ENST00000372325.6:c.653G>T	ENSP00000361400.2:p.Gly218Val
ENST00000372327.9:c.653G>T	ENSP00000361402.5:p.Gly218Val
NM_001098668.2:c.653G>T	NP_001092138.1:p.Gly218Val
XM_005270128.2:c.704G>T	XP_005270185.1:p.Gly235Val
XM_005270131.3:c.653G>T	XP_005270188.1:p.Gly218Val
XM_005270132.3:c.653G>T	XP_005270189.1:p.Gly218Val
XM_011540124.1:c.653G>T	XP_011538426.1:p.Gly218Val
XM_011540125.1:c.653G>T	XP_011538427.1:p.Gly218Val
NM_001098668.3:c.653G>T	NP_001092138.1:p.Gly218Val
NM_001320813.1:c.653G>T	NP_001307742.1:p.Gly218Val
NM_001320814.1:c.683G>T	NP_001307743.1:p.Gly228Val
XM_005270128.3:c.704G>T	XP_005270185.1:p.Gly235Val
XM_017016608.1:c.653G>T	XP_016872097.1:p.Gly218Val
NM_001098668.4:c.653G>T MANE Select	NP_001092138.1:p.Gly218Val
NM_001320813.2:c.653G>T	NP_001307742.1:p.Gly218Val