Canonical Allele Identifier: CA350096320

Gene: CRYGC

Linked Data

• MyVariant Identifiers: chr2:g.208994208A>T (hg19) ; chr2:g.208129484A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129484A>T , CM000664.2:g.208129484A>T	GRCh38
NC_000002.11:g.208994208A>T , CM000664.1:g.208994208A>T	GRCh37
NC_000002.10:g.208702453A>T	NCBI36
NG_008038.1:g.5347T>A
NG_008039.1:g.106T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.209T>A MANE Select	ENSP00000282141.3:p.Met70Lys
ENST00000282141.3:c.209T>A	ENSP00000282141.3:p.Met70Lys
NM_020989.3:c.209T>A	NP_066269.1:p.Met70Lys
NR_038437.1:n.98-7572A>T
XM_011510661.1:c.209T>A	XP_011508963.1:p.Met70Lys
XM_011510662.1:c.209T>A	XP_011508964.1:p.Met70Lys
XM_011510663.1:c.80T>A	XP_011508965.1:p.Met27Lys
NM_020989.4:c.209T>A MANE Select	NP_066269.1:p.Met70Lys