Canonical Allele Identifier: CA223009851

Gene: SCGB1A1

Linked Data

• dbSNP Id: rs867068307
• gnomAD v3: 11-62418995-C-T
• gnomAD v4: 11-62418995-C-T
• MyVariant Identifiers: chr11:g.62186467C>T (hg19) ; chr11:g.62418995C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62418995C>T , CM000673.2:g.62418995C>T	GRCh38
NC_000011.9:g.62186467C>T , CM000673.1:g.62186467C>T	GRCh37
NC_000011.8:g.61943043C>T	NCBI36
NG_021331.1:g.4961C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534397.5:c.-51+2358C>T	ENSP00000432866.1:n.-51+2358C>T
XR_950170.1:n.378-2145G>A
XR_950171.1:n.234-2145G>A
XR_950172.1:n.234-2145G>A
XR_950173.1:n.234-2145G>A
XR_950174.1:n.234-2145G>A
XR_001748247.1:n.348-2145G>A
XR_001748248.1:n.453-2145G>A
XR_001748249.1:n.459-2145G>A
XR_001748250.1:n.455-2145G>A
XR_001748252.1:n.460-2145G>A
XR_001748253.1:n.180-2145G>A
XR_001748254.1:n.461-2145G>A
XR_002957250.1:n.451-2145G>A