Canonical Allele Identifier: CA2077991

Gene: CRYGC

Linked Data

• dbSNP Id: rs768377987
• ExAC: 2:208994473 T / A
• gnomAD v2: 2-208994473-T-A
• gnomAD v3: 2-208129749-T-A
• gnomAD v4: 2-208129749-T-A
• MyVariant Identifiers: chr2:g.208994473T>A (hg19) ; chr2:g.208129749T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129749T>A , CM000664.2:g.208129749T>A	GRCh38
NC_000002.11:g.208994473T>A , CM000664.1:g.208994473T>A	GRCh37
NC_000002.10:g.208702718T>A	NCBI36
NG_008038.1:g.5082A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.9+35A>T MANE Select	ENSP00000282141.3:n.9+35A>T
ENST00000282141.3:c.9+35A>T	ENSP00000282141.3:n.9+35A>T
NM_020989.3:c.9+35A>T	NP_066269.1:n.9+35A>T
NR_038437.1:n.98-7307T>A
XM_011510661.1:c.9+35A>T	XP_011508963.1:n.9+35A>T
XM_011510662.1:c.9+35A>T	XP_011508964.1:n.9+35A>T
XM_011510663.1:c.-120-66A>T	XP_011508965.1:n.-120-66A>T
NM_020989.4:c.9+35A>T MANE Select	NP_066269.1:n.9+35A>T