Canonical Allele Identifier: CA1030381914
Gene: STON1-GTF2A1L HGNC NCBI
LHCGR HGNC NCBI

Linked Data

dbSNP Id: rs1572905470
gnomAD v3: 2-48755734-A-C
gnomAD v4: 2-48755734-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48755734A>C , CM000664.2:g.48755734A>C GRCh38
NC_000002.11:g.48982873A>C , CM000664.1:g.48982873A>C GRCh37
NC_000002.10:g.48836377A>C NCBI36
NG_008193.1:g.5008T>G
NG_033050.1:g.230810A>C
NG_008193.2:g.5008T>G
NG_033050.2:g.230810A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000402114.6:c.3442-20546A>C (STON1-GTF2A1L) ENSP00000385701.1:n.3442-20546A>C
NM_000233.3:c.-63T>G (LHCGR) NP_000224.2:n.-63T>G
NM_001198593.1:c.3442-20546A>C (STON1-GTF2A1L) NP_001185522.1:n.3442-20546A>C
NM_001198593.2:c.3442-20546A>C (STON1-GTF2A1L) NP_001185522.1:n.3442-20546A>C