Canonical Allele Identifier: CA1030381765

Gene: LHCGR STON1-GTF2A1L

Linked Data

• dbSNP Id: rs1670164843
• gnomAD v3: 2-48755477-C-T
• gnomAD v4: 2-48755477-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48755477C>T , CM000664.2:g.48755477C>T	GRCh38
NC_000002.11:g.48982616C>T , CM000664.1:g.48982616C>T	GRCh37
NC_000002.10:g.48836120C>T	NCBI36
NG_008193.1:g.5265G>A
NG_033050.1:g.230553C>T
NG_008193.2:g.5265G>A
NG_033050.2:g.230553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.161+34G>A (LHCGR) MANE Select	ENSP00000294954.6:n.161+34G>A
ENST00000294954.11:c.161+34G>A (LHCGR)	ENSP00000294954.6:n.161+34G>A
ENST00000401907.5:c.161+34G>A (LHCGR)	ENSP00000385406.1:n.161+34G>A
ENST00000402114.6:c.3442-20803C>T (STON1-GTF2A1L)	ENSP00000385701.1:n.3442-20803C>T
ENST00000403273.5:c.161+34G>A (LHCGR)	ENSP00000385847.1:n.161+34G>A
ENST00000405626.5:c.161+34G>A (LHCGR)	ENSP00000386033.1:n.161+34G>A
ENST00000428232.2:c.59+34G>A (LHCGR)	ENSP00000403748.1:n.59+34G>A
ENST00000602369.3:c.161+34G>A	ENSP00000473498.1:n.161+34G>A
NM_000233.3:c.161+34G>A (LHCGR)	NP_000224.2:n.161+34G>A
NM_001198593.1:c.3442-20803C>T (STON1-GTF2A1L)	NP_001185522.1:n.3442-20803C>T
XM_011532828.1:c.161+34G>A (LHCGR)	XP_011531130.1:n.161+34G>A
XM_011532829.1:c.161+34G>A (LHCGR)	XP_011531131.1:n.161+34G>A
XM_011532830.1:c.161+34G>A (LHCGR)	XP_011531132.1:n.161+34G>A
NM_000233.4:c.161+34G>A (LHCGR) MANE Select	NP_000224.2:n.161+34G>A
NM_001198593.2:c.3442-20803C>T (STON1-GTF2A1L)	NP_001185522.1:n.3442-20803C>T