Canonical Allele Identifier: CA1922436784
Gene: SFTPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79976225A= , CM000672.2:g.79976225A= GRCh38
NC_000010.10:g.81735981A= , CM000672.1:g.81735981A= GRCh37
NC_000010.9:g.81725961A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000444384.3:c.36+6350T= ENSP00000394325.1:n.36+6350T=
XM_011540087.1:c.-4+5993T= XP_011538389.1:n.-4+5993T=