Canonical Allele Identifier: CA1323931624

Gene: CRYGC

Linked Data

• dbSNP Id: rs1695075817
• gnomAD v4: 2-208129903-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129903C>T , CM000664.2:g.208129903C>T	GRCh38
NC_000002.11:g.208994627C>T , CM000664.1:g.208994627C>T	GRCh37
NC_000002.10:g.208702872C>T	NCBI36
NG_008038.1:g.4928G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_038437.1:n.98-7153C>T
XM_011510661.1:c.-79-32G>A	XP_011508963.1:n.-79-32G>A
XM_011510662.1:c.-79-32G>A	XP_011508964.1:n.-79-32G>A
XM_011510663.1:c.-120-220G>A	XP_011508965.1:n.-120-220G>A