Canonical Allele Identifier: CA223009856
Gene: SCGB1A1 HGNC NCBI

Linked Data

dbSNP Id: rs567388364
gnomAD v2: 11-62186476-T-C
gnomAD v3: 11-62419004-T-C
gnomAD v4: 11-62419004-T-C
MyVariant Identifiers: chr11:g.62186476T>C (hg19) chr11:g.62419004T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62419004T>C , CM000673.2:g.62419004T>C GRCh38
NC_000011.9:g.62186476T>C , CM000673.1:g.62186476T>C GRCh37
NC_000011.8:g.61943052T>C NCBI36
NG_021331.1:g.4970T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000534397.5:c.-51+2367T>C ENSP00000432866.1:n.-51+2367T>C
XR_950170.1:n.378-2154A>G
XR_950171.1:n.234-2154A>G
XR_950172.1:n.234-2154A>G
XR_950173.1:n.234-2154A>G
XR_950174.1:n.234-2154A>G
XR_001748247.1:n.348-2154A>G
XR_001748248.1:n.453-2154A>G
XR_001748249.1:n.459-2154A>G
XR_001748250.1:n.455-2154A>G
XR_001748252.1:n.460-2154A>G
XR_001748253.1:n.180-2154A>G
XR_001748254.1:n.461-2154A>G
XR_002957250.1:n.451-2154A>G
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