Canonical Allele Identifier: CA1977752110
Gene: SCGB1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62419080A= , CM000673.2:g.62419080A= GRCh38
NC_000011.9:g.62186552A= , CM000673.1:g.62186552A= GRCh37
NC_000011.8:g.61943128A= NCBI36
NG_021331.1:g.5046A=

Transcript Alleles

HGVS Amino-acid change
ENST00000278282.3:c.-16A= MANE Select ENSP00000278282.2:n.-16A=
ENST00000278282.2:c.-16A= ENSP00000278282.2:n.-16A=
ENST00000534397.5:c.-51+2443A= ENSP00000432866.1:n.-51+2443A=
NM_003357.4:c.-16A= NP_003348.1:n.-16A=
XR_950170.1:n.378-2230T=
XR_950171.1:n.234-2230T=
XR_950172.1:n.234-2230T=
XR_950173.1:n.234-2230T=
XR_950174.1:n.234-2230T=
XR_001748247.1:n.348-2230T=
XR_001748248.1:n.453-2230T=
XR_001748249.1:n.459-2230T=
XR_001748250.1:n.455-2230T=
XR_001748252.1:n.460-2230T=
XR_001748253.1:n.180-2230T=
XR_001748254.1:n.461-2230T=
XR_002957250.1:n.451-2230T=
NM_003357.5:c.-16A= MANE Select NP_003348.1:n.-16A=