Canonical Allele Identifier: CA806152752

Gene: SGCD

Linked Data

• dbSNP Id: rs1257875285
• MyVariant Identifiers: chr5:g.156193972G>C (hg19) ; chr5:g.156766961G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156766961G>C , CM000667.2:g.156766961G>C	GRCh38
NC_000005.9:g.156193972G>C , CM000667.1:g.156193972G>C	GRCh37
NC_000005.8:g.156126550G>C	NCBI36
NG_008693.2:g.901619G>C , LRG_205:g.901619G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.*7571G>C MANE Select	ENSP00000338343.4:n.*7571G>C
ENST00000435422.7:c.*7571G>C	ENSP00000403003.2:n.*7571G>C
NM_000337.5:c.*7571G>C , LRG_205t1:c.*7571G>C	NP_000328.2:n.*7571G>C
NM_001128209.1:c.*7571G>C	NP_001121681.1:n.*7571G>C
XM_005265966.3:c.*7571G>C	XP_005266023.1:n.*7571G>C
XM_006714911.2:c.*7571G>C	XP_006714974.1:n.*7571G>C
XM_011534621.1:c.*7571G>C	XP_011532923.1:n.*7571G>C
NM_001128209.2:c.*7571G>C	NP_001121681.1:n.*7571G>C
NM_000337.6:c.*7571G>C MANE Select	NP_000328.2:n.*7571G>C