Canonical Allele Identifier: CA938669402
Gene: SCGB1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1937709930
gnomAD v3: 11-62418902-A-C
gnomAD v4: 11-62418902-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62418902A>C , CM000673.2:g.62418902A>C GRCh38
NC_000011.9:g.62186374A>C , CM000673.1:g.62186374A>C GRCh37
NC_000011.8:g.61942950A>C NCBI36
NG_021331.1:g.4868A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000534397.5:c.-51+2265A>C ENSP00000432866.1:n.-51+2265A>C
XR_950170.1:n.378-2052T>G
XR_950171.1:n.234-2052T>G
XR_950172.1:n.234-2052T>G
XR_950173.1:n.234-2052T>G
XR_950174.1:n.234-2052T>G
XR_001748247.1:n.348-2052T>G
XR_001748248.1:n.453-2052T>G
XR_001748249.1:n.459-2052T>G
XR_001748250.1:n.455-2052T>G
XR_001748252.1:n.460-2052T>G
XR_001748253.1:n.180-2052T>G
XR_001748254.1:n.461-2052T>G
XR_002957250.1:n.451-2052T>G
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