Canonical Allele Identifier: CA938669404
Gene: SCGB1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1937710138

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62418914C>G , CM000673.2:g.62418914C>G GRCh38
NC_000011.9:g.62186386C>G , CM000673.1:g.62186386C>G GRCh37
NC_000011.8:g.61942962C>G NCBI36
NG_021331.1:g.4880C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000534397.5:c.-51+2277C>G ENSP00000432866.1:n.-51+2277C>G
XR_950170.1:n.378-2064G>C
XR_950171.1:n.234-2064G>C
XR_950172.1:n.234-2064G>C
XR_950173.1:n.234-2064G>C
XR_950174.1:n.234-2064G>C
XR_001748247.1:n.348-2064G>C
XR_001748248.1:n.453-2064G>C
XR_001748249.1:n.459-2064G>C
XR_001748250.1:n.455-2064G>C
XR_001748252.1:n.460-2064G>C
XR_001748253.1:n.180-2064G>C
XR_001748254.1:n.461-2064G>C
XR_002957250.1:n.451-2064G>C