Canonical Allele Identifier: CA567762208

Gene: EYS

Linked Data

• dbSNP Id: rs1186389924
• gnomAD v2: 6-65767383-C-G
• gnomAD v3: 6-65057490-C-G
• gnomAD v4: 6-65057490-C-G
• MyVariant Identifiers: chr6:g.65767383C>G (hg19) ; chr6:g.65057490C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.65057490C>G , CM000668.2:g.65057490C>G	GRCh38
NC_000006.11:g.65767383C>G , CM000668.1:g.65767383C>G	GRCh37
NC_000006.10:g.65824104C>G	NCBI36
NG_023443.1:g.654736G>C
NG_023443.2:g.654736G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.2137+124G>C MANE Select	ENSP00000424243.1:n.2137+124G>C
ENST00000370616.6:c.2137+124G>C	ENSP00000359650.2:n.2137+124G>C
ENST00000370618.7:c.2137+124G>C	ENSP00000359652.4:n.2137+124G>C
ENST00000370621.7:c.2137+124G>C	ENSP00000359655.3:n.2137+124G>C
ENST00000503581.5:c.2137+124G>C	ENSP00000424243.1:n.2137+124G>C
NM_001142800.1:c.2137+124G>C	NP_001136272.1:n.2137+124G>C
NM_001292009.1:c.2137+124G>C	NP_001278938.1:n.2137+124G>C
NM_001142800.2:c.2137+124G>C MANE Select	NP_001136272.1:n.2137+124G>C
NM_001292009.2:c.2137+124G>C	NP_001278938.1:n.2137+124G>C