Canonical Allele Identifier: CA1652953
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI
GTF2A1L HGNC NCBI

Linked Data

dbSNP Id: rs200467316
gnomAD v2: 2-48914951-T-C
gnomAD v3: 2-48687812-T-C
gnomAD v4: 2-48687812-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48687812T>C , CM000664.2:g.48687812T>C GRCh38
NC_000002.11:g.48914951T>C , CM000664.1:g.48914951T>C GRCh37
NC_000002.10:g.48768455T>C NCBI36
NG_008193.1:g.72930A>G
NG_033050.1:g.162888T>C
NG_008193.2:g.72930A>G
NG_033050.2:g.162888T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000294954.12:c.1985A>G (LHCGR) MANE Select ENSP00000294954.6:p.Asn662Ser
ENST00000294954.11:c.1985A>G (LHCGR) ENSP00000294954.6:p.Asn662Ser
ENST00000401907.5:c.*297A>G (LHCGR) ENSP00000385406.1:n.*297A>G
ENST00000402114.6:c.3441+16132T>C (STON1-GTF2A1L) ENSP00000385701.1:n.3441+16132T>C
ENST00000403273.5:c.*729A>G (LHCGR) ENSP00000385847.1:n.*729A>G
ENST00000405626.5:c.1904A>G (LHCGR) ENSP00000386033.1:p.Asn635Ser
ENST00000508440.1:c.276+16132T>C (GTF2A1L) ENSP00000421474.1:n.276+16132T>C
ENST00000602369.3:c.*220+6412A>G ENSP00000473498.1:n.*220+6412A>G
NM_000233.3:c.1985A>G (LHCGR) NP_000224.2:p.Asn662Ser
NM_001198593.1:c.3441+16132T>C (STON1-GTF2A1L) NP_001185522.1:n.3441+16132T>C
XM_005264309.2:c.1028A>G (LHCGR) XP_005264366.1:p.Asn343Ser
XM_006712015.2:c.1055A>G (LHCGR) XP_006712078.1:p.Asn352Ser
XM_011532828.1:c.1910A>G (LHCGR) XP_011531130.1:p.Asn637Ser
XM_011532829.1:c.1724A>G (LHCGR) XP_011531131.1:p.Asn575Ser
XM_011532830.1:c.1643A>G (LHCGR) XP_011531132.1:p.Asn548Ser
XM_011532831.1:c.1349A>G (LHCGR) XP_011531133.1:p.Asn450Ser
XM_011532832.1:c.1055A>G (LHCGR) XP_011531134.1:p.Asn352Ser
XM_011532833.1:c.1055A>G (LHCGR) XP_011531135.1:p.Asn352Ser
XM_011532834.1:c.1028A>G (LHCGR) XP_011531136.1:p.Asn343Ser
XM_005264309.3:c.1028A>G (LHCGR) XP_005264366.1:p.Asn343Ser
XM_006712015.3:c.1055A>G (LHCGR) XP_006712078.1:p.Asn352Ser
XM_011532834.2:c.1028A>G (LHCGR) XP_011531136.1:p.Asn343Ser
XM_017004089.1:c.1730A>G (LHCGR) XP_016859578.1:p.Asn577Ser
XM_017004090.1:c.1349A>G (LHCGR) XP_016859579.1:p.Asn450Ser
NM_000233.4:c.1985A>G (LHCGR) MANE Select NP_000224.2:p.Asn662Ser
NM_001198593.2:c.3441+16132T>C (STON1-GTF2A1L) NP_001185522.1:n.3441+16132T>C