Canonical Allele Identifier: CA350097687
Gene: CRYGC HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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