Canonical Allele Identifier: CA350096655

Gene: CRYGC

Linked Data

• MyVariant Identifiers: chr2:g.208994235C>A (hg19) ; chr2:g.208129511C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129511C>A , CM000664.2:g.208129511C>A	GRCh38
NC_000002.11:g.208994235C>A , CM000664.1:g.208994235C>A	GRCh37
NC_000002.10:g.208702480C>A	NCBI36
NG_008038.1:g.5320G>T
NG_008039.1:g.79G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.182G>T MANE Select	ENSP00000282141.3:p.Gly61Val
ENST00000282141.3:c.182G>T	ENSP00000282141.3:p.Gly61Val
NM_020989.3:c.182G>T	NP_066269.1:p.Gly61Val
NR_038437.1:n.98-7545C>A
XM_011510661.1:c.182G>T	XP_011508963.1:p.Gly61Val
XM_011510662.1:c.182G>T	XP_011508964.1:p.Gly61Val
XM_011510663.1:c.53G>T	XP_011508965.1:p.Gly18Val
NM_020989.4:c.182G>T MANE Select	NP_066269.1:p.Gly61Val