Canonical Allele Identifier: CA1977752107

Gene: SCGB1A1

Linked Data

• dbSNP Id: rs1937713851
• gnomAD v4: 11-62419076-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62419076G>C , CM000673.2:g.62419076G>C	GRCh38
NC_000011.9:g.62186548G>C , CM000673.1:g.62186548G>C	GRCh37
NC_000011.8:g.61943124G>C	NCBI36
NG_021331.1:g.5042G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278282.3:c.-20G>C MANE Select	ENSP00000278282.2:n.-20G>C
ENST00000278282.2:c.-20G>C	ENSP00000278282.2:n.-20G>C
ENST00000534397.5:c.-51+2439G>C	ENSP00000432866.1:n.-51+2439G>C
NM_003357.4:c.-20G>C	NP_003348.1:n.-20G>C
XR_950170.1:n.378-2226C>G
XR_950171.1:n.234-2226C>G
XR_950172.1:n.234-2226C>G
XR_950173.1:n.234-2226C>G
XR_950174.1:n.234-2226C>G
XR_001748247.1:n.348-2226C>G
XR_001748248.1:n.453-2226C>G
XR_001748249.1:n.459-2226C>G
XR_001748250.1:n.455-2226C>G
XR_001748252.1:n.460-2226C>G
XR_001748253.1:n.180-2226C>G
XR_001748254.1:n.461-2226C>G
XR_002957250.1:n.451-2226C>G
NM_003357.5:c.-20G>C MANE Select	NP_003348.1:n.-20G>C