Canonical Allele Identifier: CA2613948592

Gene: SCGB1A1

Linked Data

• gnomAD v4: 11-62419082-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62419082C>T , CM000673.2:g.62419082C>T	GRCh38
NC_000011.9:g.62186554C>T , CM000673.1:g.62186554C>T	GRCh37
NC_000011.8:g.61943130C>T	NCBI36
NG_021331.1:g.5048C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278282.3:c.-14C>T MANE Select	ENSP00000278282.2:n.-14C>T
ENST00000278282.2:c.-14C>T	ENSP00000278282.2:n.-14C>T
ENST00000534397.5:c.-51+2445C>T	ENSP00000432866.1:n.-51+2445C>T
NM_003357.4:c.-14C>T	NP_003348.1:n.-14C>T
XR_950170.1:n.378-2232G>A
XR_950171.1:n.234-2232G>A
XR_950172.1:n.234-2232G>A
XR_950173.1:n.234-2232G>A
XR_950174.1:n.234-2232G>A
XR_001748247.1:n.348-2232G>A
XR_001748248.1:n.453-2232G>A
XR_001748249.1:n.459-2232G>A
XR_001748250.1:n.455-2232G>A
XR_001748252.1:n.460-2232G>A
XR_001748253.1:n.180-2232G>A
XR_001748254.1:n.461-2232G>A
XR_002957250.1:n.451-2232G>A
NM_003357.5:c.-14C>T MANE Select	NP_003348.1:n.-14C>T