Canonical Allele Identifier: CA1977752133
Gene: SCGB1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62419093A= , CM000673.2:g.62419093A= GRCh38
NC_000011.9:g.62186565A= , CM000673.1:g.62186565A= GRCh37
NC_000011.8:g.61943141A= NCBI36
NG_021331.1:g.5059A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278282.3:c.-3A= MANE Select ENSP00000278282.2:n.-3A=
ENST00000278282.2:c.-3A= ENSP00000278282.2:n.-3A=
ENST00000534397.5:c.-51+2456A= ENSP00000432866.1:n.-51+2456A=
NM_003357.4:c.-3A= NP_003348.1:n.-3A=
XR_950170.1:n.378-2243T=
XR_950171.1:n.234-2243T=
XR_950172.1:n.234-2243T=
XR_950173.1:n.234-2243T=
XR_950174.1:n.234-2243T=
XR_001748247.1:n.348-2243T=
XR_001748248.1:n.453-2243T=
XR_001748249.1:n.459-2243T=
XR_001748250.1:n.455-2243T=
XR_001748252.1:n.460-2243T=
XR_001748253.1:n.180-2243T=
XR_001748254.1:n.461-2243T=
XR_002957250.1:n.451-2243T=
NM_003357.5:c.-3A= MANE Select NP_003348.1:n.-3A=