Canonical Allele Identifier: CA372625646

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1554873895
• gnomAD v2: 8-145641394-A-G
• gnomAD v4: 8-144416010-A-G
• MyVariant Identifiers: chr8:g.145641394A>G (hg19) ; chr8:g.144416010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144416010A>G , CM000670.2:g.144416010A>G	GRCh38
NC_000008.10:g.145641394A>G , CM000670.1:g.145641394A>G	GRCh37
NC_000008.9:g.145612202A>G	NCBI36
NG_012234.2:g.5881T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301305.8:c.274T>C MANE Select	ENSP00000301305.4:p.Tyr92His
ENST00000276833.9:c.199T>C	ENSP00000276833.5:p.Tyr67His
ENST00000301305.7:c.274T>C	ENSP00000301305.3:p.Tyr92His
ENST00000526658.1:c.192+588T>C	ENSP00000434512.1:n.192+588T>C
NM_017767.2:c.199T>C	NP_060237.2:p.Tyr67His
NM_130849.3:c.274T>C	NP_570901.2:p.Tyr92His
XM_006716599.1:c.274T>C	XP_006716662.1:p.Tyr92His
XM_011517153.1:c.192+588T>C	XP_011515455.1:n.192+588T>C
XM_024447188.1:c.192+588T>C	XP_024302956.1:n.192+588T>C
XM_024447189.1:c.192+588T>C	XP_024302957.1:n.192+588T>C
NM_001374839.1:c.192+588T>C	NP_001361768.1:n.192+588T>C
NM_017767.3:c.199T>C	NP_060237.3:p.Tyr67His
NM_130849.4:c.274T>C MANE Select	NP_570901.3:p.Tyr92His