Canonical Allele Identifier: CA2014342486

Gene: EMG1

Linked Data

• dbSNP Id: rs1946365764
• gnomAD v4: 12-6974241-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974241G>T , CM000674.2:g.6974241G>T	GRCh38
NC_000012.11:g.7083403G>T , CM000674.1:g.7083403G>T	GRCh37
NC_000012.10:g.6953664G>T	NCBI36
NG_021408.1:g.8461G>T
NG_021408.2:g.8461G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.169-98G>T MANE Select	ENSP00000470560.1:n.169-98G>T
ENST00000261406.7:c.151-98G>T	ENSP00000476966.2:n.151-98G>T
ENST00000539196.2:c.32-98G>T
ENST00000599672.5:c.169-98G>T	ENSP00000470560.1:n.169-98G>T
ENST00000607161.5:c.172-98G>T	ENSP00000480420.1:n.172-98G>T
ENST00000611981.1:n.180-98G>T
ENST00000620255.1:n.158-98G>T
NM_006331.7:c.169-98G>T	NP_006322.4:n.169-98G>T
XM_011520907.1:c.169-98G>T	XP_011519209.1:n.169-98G>T
NM_001320049.1:c.169-98G>T	NP_001306978.1:n.169-98G>T
NR_135131.1:n.312-98G>T
NM_006331.8:c.169-98G>T MANE Select	NP_006322.4:n.169-98G>T
NM_001320049.2:c.169-98G>T	NP_001306978.1:n.169-98G>T
NR_135131.2:n.180-98G>T