Canonical Allele Identifier: CA894035015

Gene: GGCX

Linked Data

• dbSNP Id: rs1236377128
• MyVariant Identifiers: chr2:g.85773715C>G (hg19) ; chr2:g.85546592C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546592C>G , CM000664.2:g.85546592C>G	GRCh38
NC_000002.11:g.85773715C>G , CM000664.1:g.85773715C>G	GRCh37
NC_000002.10:g.85627226C>G	NCBI36
NG_011811.2:g.19943G>C
NG_029183.1:g.12615C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3342G>C MANE Select	ENSP00000233838.3:n.*3342G>C
ENST00000233838.8:c.*3342G>C	ENSP00000233838.3:n.*3342G>C
NM_000821.5:c.*3342G>C	NP_000812.2:n.*3342G>C
NM_000821.6:c.*3342G>C	NP_000812.2:n.*3342G>C
NM_001142269.2:c.*3342G>C	NP_001135741.1:n.*3342G>C
NM_001142269.3:c.*3342G>C	NP_001135741.1:n.*3342G>C
NM_000821.7:c.*3342G>C MANE Select	NP_000812.2:n.*3342G>C
NM_001142269.4:c.*3342G>C	NP_001135741.1:n.*3342G>C