Canonical Allele Identifier: CA146179274

Gene: HS3ST5 HDAC2-AS2

Linked Data

• dbSNP Id: rs1054459649
• gnomAD v3: 6-114301070-G-C
• gnomAD v4: 6-114301070-G-C
• MyVariant Identifiers: chr6:g.114622234G>C (hg19) ; chr6:g.114301070G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.114301070G>C , CM000668.2:g.114301070G>C	GRCh38
NC_000006.11:g.114622234G>C , CM000668.1:g.114622234G>C	GRCh37
NC_000006.10:g.114728927G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312719.10:c.-339+41125C>G (HS3ST5) MANE Select	ENSP00000427888.1:n.-339+41125C>G
ENST00000312719.9:c.-339+41125C>G (HS3ST5)	ENSP00000427888.1:n.-339+41125C>G
NR_125845.1:n.1800-39452G>C (HDAC2-AS2)
XM_006715379.2:c.-339+41125C>G (HS3ST5)	XP_006715442.1:n.-339+41125C>G
XM_011535587.1:c.-339+40302C>G (HS3ST5)	XP_011533889.1:n.-339+40302C>G
XR_942347.1:n.239+41125C>G (HS3ST5)
XM_017010470.1:c.-339+40302C>G (HS3ST5)	XP_016865959.1:n.-339+40302C>G
XM_017010473.1:c.-335+40302C>G (HS3ST5)	XP_016865962.1:n.-335+40302C>G
XM_017010474.2:c.-335+41125C>G (HS3ST5)	XP_016865963.1:n.-335+41125C>G
NM_001387039.1:c.-227+40302C>G (HS3ST5)	NP_001373968.1:n.-227+40302C>G
NM_001387040.1:c.-33+41125C>G (HS3ST5)	NP_001373969.1:n.-33+41125C>G
NM_001387041.1:c.-335+41125C>G (HS3ST5)	NP_001373970.1:n.-335+41125C>G
NM_001387042.1:c.-339+40302C>G (HS3ST5)	NP_001373971.1:n.-339+40302C>G
NM_001387043.1:c.-335+40302C>G (HS3ST5)	NP_001373972.1:n.-335+40302C>G
NM_001387044.1:c.-429+41125C>G (HS3ST5)	NP_001373973.1:n.-429+41125C>G
NM_001387045.1:c.-434+41125C>G (HS3ST5)	NP_001373974.1:n.-434+41125C>G
NM_001387046.1:c.-227+41125C>G (HS3ST5)	NP_001373975.1:n.-227+41125C>G
NM_001387047.1:c.-434+40302C>G (HS3ST5)	NP_001373976.1:n.-434+40302C>G
NM_153612.4:c.-339+41125C>G (HS3ST5) MANE Select	NP_705840.2:n.-339+41125C>G