Canonical Allele Identifier: CA214750

Gene: SCGB1A1

Linked Data

• MyVariant Identifiers: chr11:g.62186530G>G (hg19) ; chr11:g.62419058G>G (hg38)
• PubMed: PMID:9550363 ; PMID:9643286 ; PMID:12100044

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62419058G= , CM000673.2:g.62419058G=	GRCh38
NC_000011.9:g.62186530G= , CM000673.1:g.62186530G=	GRCh37
NC_000011.8:g.61943106G=	NCBI36
NG_021331.1:g.5024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278282.3:c.-38G= MANE Select	ENSP00000278282.2:n.-38G=
ENST00000278282.2:c.-38G=	ENSP00000278282.2:n.-38G=
ENST00000534397.5:c.-51+2421G=	ENSP00000432866.1:n.-51+2421G=
NM_003357.4:c.-38G=	NP_003348.1:n.-38G=
XR_950170.1:n.378-2208C=
XR_950171.1:n.234-2208C=
XR_950172.1:n.234-2208C=
XR_950173.1:n.234-2208C=
XR_950174.1:n.234-2208C=
XR_001748247.1:n.348-2208C=
XR_001748248.1:n.453-2208C=
XR_001748249.1:n.459-2208C=
XR_001748250.1:n.455-2208C=
XR_001748252.1:n.460-2208C=
XR_001748253.1:n.180-2208C=
XR_001748254.1:n.461-2208C=
XR_002957250.1:n.451-2208C=
NM_003357.5:c.-38G= MANE Select	NP_003348.1:n.-38G=