Canonical Allele Identifier: CA6043375
Gene: SCGB1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027621
ClinVar RCV Id: RCV001328408
dbSNP Id: rs3741240

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62419070G>A , CM000673.2:g.62419070G>A GRCh38
NC_000011.9:g.62186542G>A , CM000673.1:g.62186542G>A GRCh37
NC_000011.8:g.61943118G>A NCBI36
NG_021331.1:g.5036G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000278282.3:c.-26G>A MANE Select ENSP00000278282.2:p.=
ENST00000278282.2:c.-26G>A ENSP00000278282.2:p.=
ENST00000534397.5:c.-51+2433G>A ENSP00000432866.1:p.=
NM_003357.4:c.-26G>A NP_003348.1:p.=
XR_950170.1:n.378-2220C>T
XR_950171.1:n.234-2220C>T
XR_950172.1:n.234-2220C>T
XR_950173.1:n.234-2220C>T
XR_950174.1:n.234-2220C>T
XR_001748247.1:n.348-2220C>T
XR_001748248.1:n.453-2220C>T
XR_001748249.1:n.459-2220C>T
XR_001748250.1:n.455-2220C>T
XR_001748252.1:n.460-2220C>T
XR_001748253.1:n.180-2220C>T
XR_001748254.1:n.461-2220C>T
XR_002957250.1:n.451-2220C>T
NM_003357.5:c.-26G>A MANE Select NP_003348.1:p.=