Canonical Allele Identifier: CA2792358731
Gene: SCGB1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62419081T>G , CM000673.2:g.62419081T>G GRCh38
NC_000011.9:g.62186553T>G , CM000673.1:g.62186553T>G GRCh37
NC_000011.8:g.61943129T>G NCBI36
NG_021331.1:g.5047T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278282.3:c.-15T>G MANE Select ENSP00000278282.2:n.-15T>G
ENST00000278282.2:c.-15T>G ENSP00000278282.2:n.-15T>G
ENST00000534397.5:c.-51+2444T>G ENSP00000432866.1:n.-51+2444T>G
NM_003357.4:c.-15T>G NP_003348.1:n.-15T>G
XR_950170.1:n.378-2231A>C
XR_950171.1:n.234-2231A>C
XR_950172.1:n.234-2231A>C
XR_950173.1:n.234-2231A>C
XR_950174.1:n.234-2231A>C
XR_001748247.1:n.348-2231A>C
XR_001748248.1:n.453-2231A>C
XR_001748249.1:n.459-2231A>C
XR_001748250.1:n.455-2231A>C
XR_001748252.1:n.460-2231A>C
XR_001748253.1:n.180-2231A>C
XR_001748254.1:n.461-2231A>C
XR_002957250.1:n.451-2231A>C
NM_003357.5:c.-15T>G MANE Select NP_003348.1:n.-15T>G