Canonical Allele Identifier: CA426095148

Gene: LHCGR STON1-GTF2A1L

Linked Data

• dbSNP Id: rs1228233692
• gnomAD v2: 2-48982670-G-A
• gnomAD v3: 2-48755531-G-A
• gnomAD v4: 2-48755531-G-A
• MyVariant Identifiers: chr2:g.48982670G>A (hg19) ; chr2:g.48755531G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48755531G>A , CM000664.2:g.48755531G>A	GRCh38
NC_000002.11:g.48982670G>A , CM000664.1:g.48982670G>A	GRCh37
NC_000002.10:g.48836174G>A	NCBI36
NG_008193.1:g.5211C>T
NG_033050.1:g.230607G>A
NG_008193.2:g.5211C>T
NG_033050.2:g.230607G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.141C>T (LHCGR) MANE Select	ENSP00000294954.6:p.Pro47=
ENST00000294954.11:c.141C>T (LHCGR)	ENSP00000294954.6:p.Pro47=
ENST00000401907.5:c.141C>T (LHCGR)	ENSP00000385406.1:p.Pro47=
ENST00000402114.6:c.3442-20749G>A (STON1-GTF2A1L)	ENSP00000385701.1:n.3442-20749G>A
ENST00000403273.5:c.141C>T (LHCGR)	ENSP00000385847.1:p.Pro47=
ENST00000405626.5:c.141C>T (LHCGR)	ENSP00000386033.1:p.Pro47=
ENST00000428232.2:c.39C>T (LHCGR)	ENSP00000403748.1:p.Pro13=
ENST00000602369.3:c.141C>T	ENSP00000473498.1:p.Pro47=
NM_000233.3:c.141C>T (LHCGR)	NP_000224.2:p.Pro47=
NM_001198593.1:c.3442-20749G>A (STON1-GTF2A1L)	NP_001185522.1:n.3442-20749G>A
XM_011532828.1:c.141C>T (LHCGR)	XP_011531130.1:p.Pro47=
XM_011532829.1:c.141C>T (LHCGR)	XP_011531131.1:p.Pro47=
XM_011532830.1:c.141C>T (LHCGR)	XP_011531132.1:p.Pro47=
NM_000233.4:c.141C>T (LHCGR) MANE Select	NP_000224.2:p.Pro47=
NM_001198593.2:c.3442-20749G>A (STON1-GTF2A1L)	NP_001185522.1:n.3442-20749G>A