Canonical Allele Identifier: CA350097688

Gene: CRYGC

Linked Data

• MyVariant Identifiers: chr2:g.208994408C>G (hg19) ; chr2:g.208129684C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129684C>G , CM000664.2:g.208129684C>G	GRCh38
NC_000002.11:g.208994408C>G , CM000664.1:g.208994408C>G	GRCh37
NC_000002.10:g.208702653C>G	NCBI36
NG_008038.1:g.5147G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000282141.4:c.10-1G>C MANE Select	ENSP00000282141.3:n.10-1G>C
ENST00000282141.3:c.10-1G>C	ENSP00000282141.3:n.10-1G>C
NM_020989.3:c.10-1G>C	NP_066269.1:n.10-1G>C
NR_038437.1:n.98-7372C>G
XM_011510661.1:c.10-1G>C	XP_011508963.1:n.10-1G>C
XM_011510662.1:c.10-1G>C	XP_011508964.1:n.10-1G>C
XM_011510663.1:c.-120-1G>C	XP_011508965.1:n.-120-1G>C
NM_020989.4:c.10-1G>C MANE Select	NP_066269.1:n.10-1G>C