Canonical Allele Identifier: CA539388994

Gene: CRYGC

Linked Data

• dbSNP Id: rs1173694780
• gnomAD v2: 2-208994555-G-T
• gnomAD v4: 2-208129831-G-T
• MyVariant Identifiers: chr2:g.208994555G>T (hg19) ; chr2:g.208129831G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129831G>T , CM000664.2:g.208129831G>T	GRCh38
NC_000002.11:g.208994555G>T , CM000664.1:g.208994555G>T	GRCh37
NC_000002.10:g.208702800G>T	NCBI36
NG_008038.1:g.5000C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_038437.1:n.98-7225G>T
XM_011510661.1:c.-39C>A	XP_011508963.1:n.-39C>A
XM_011510662.1:c.-39C>A	XP_011508964.1:n.-39C>A
XM_011510663.1:c.-120-148C>A	XP_011508965.1:n.-120-148C>A