Canonical Allele Identifier: CA346742997

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• dbSNP Id: rs1009088916
• gnomAD v2: 2-48914885-T-C
• gnomAD v4: 2-48687746-T-C
• MyVariant Identifiers: chr2:g.48914885T>C (hg19) ; chr2:g.48687746T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48687746T>C , CM000664.2:g.48687746T>C	GRCh38
NC_000002.11:g.48914885T>C , CM000664.1:g.48914885T>C	GRCh37
NC_000002.10:g.48768389T>C	NCBI36
NG_008193.1:g.72996A>G
NG_033050.1:g.162822T>C
NG_008193.2:g.72996A>G
NG_033050.2:g.162822T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.2051A>G (LHCGR) MANE Select	ENSP00000294954.6:p.His684Arg
ENST00000294954.11:c.2051A>G (LHCGR)	ENSP00000294954.6:p.His684Arg
ENST00000401907.5:c.*363A>G (LHCGR)	ENSP00000385406.1:n.*363A>G
ENST00000402114.6:c.3441+16066T>C (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16066T>C
ENST00000403273.5:c.*795A>G (LHCGR)	ENSP00000385847.1:n.*795A>G
ENST00000405626.5:c.1970A>G (LHCGR)	ENSP00000386033.1:p.His657Arg
ENST00000508440.1:c.276+16066T>C (GTF2A1L)	ENSP00000421474.1:n.276+16066T>C
ENST00000602369.3:c.*220+6478A>G	ENSP00000473498.1:n.*220+6478A>G
NM_000233.3:c.2051A>G (LHCGR)	NP_000224.2:p.His684Arg
NM_001198593.1:c.3441+16066T>C (STON1-GTF2A1L)	NP_001185522.1:n.3441+16066T>C
XM_005264309.2:c.1094A>G (LHCGR)	XP_005264366.1:p.His365Arg
XM_006712015.2:c.1121A>G (LHCGR)	XP_006712078.1:p.His374Arg
XM_011532828.1:c.1976A>G (LHCGR)	XP_011531130.1:p.His659Arg
XM_011532829.1:c.1790A>G (LHCGR)	XP_011531131.1:p.His597Arg
XM_011532830.1:c.1709A>G (LHCGR)	XP_011531132.1:p.His570Arg
XM_011532831.1:c.1415A>G (LHCGR)	XP_011531133.1:p.His472Arg
XM_011532832.1:c.1121A>G (LHCGR)	XP_011531134.1:p.His374Arg
XM_011532833.1:c.1121A>G (LHCGR)	XP_011531135.1:p.His374Arg
XM_011532834.1:c.1094A>G (LHCGR)	XP_011531136.1:p.His365Arg
XM_005264309.3:c.1094A>G (LHCGR)	XP_005264366.1:p.His365Arg
XM_006712015.3:c.1121A>G (LHCGR)	XP_006712078.1:p.His374Arg
XM_011532834.2:c.1094A>G (LHCGR)	XP_011531136.1:p.His365Arg
XM_017004089.1:c.1796A>G (LHCGR)	XP_016859578.1:p.His599Arg
XM_017004090.1:c.1415A>G (LHCGR)	XP_016859579.1:p.His472Arg
NM_000233.4:c.2051A>G (LHCGR) MANE Select	NP_000224.2:p.His684Arg
NM_001198593.2:c.3441+16066T>C (STON1-GTF2A1L)	NP_001185522.1:n.3441+16066T>C