Canonical Allele Identifier: CA277624359

Gene: EMP2

Linked Data

• dbSNP Id: rs1052719950
• gnomAD v2: 16-10633172-G-C
• gnomAD v3: 16-10539315-G-C
• gnomAD v4: 16-10539315-G-C
• MyVariant Identifiers: chr16:g.10633172G>C (hg19) ; chr16:g.10539315G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539315G>C , CM000678.2:g.10539315G>C	GRCh38
NC_000016.9:g.10633172G>C , CM000678.1:g.10633172G>C	GRCh37
NC_000016.8:g.10540673G>C	NCBI36
NG_042058.1:g.46402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1241C>G MANE Select	ENSP00000352540.3:n.170-1241C>G
ENST00000359543.7:c.170-1241C>G	ENSP00000352540.3:n.170-1241C>G
ENST00000536829.1:c.170-1241C>G	ENSP00000445712.1:n.170-1241C>G
NM_001424.4:c.170-1241C>G	NP_001415.1:n.170-1241C>G
NM_001424.5:c.170-1241C>G	NP_001415.1:n.170-1241C>G
XM_006720864.2:c.170-1241C>G	XP_006720927.1:n.170-1241C>G
XM_006720864.3:c.170-1241C>G	XP_006720927.1:n.170-1241C>G
NM_001424.6:c.170-1241C>G MANE Select	NP_001415.1:n.170-1241C>G