Canonical Allele Identifier: CA577030163

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1381474115
• gnomAD v2: 7-107312559-T-C
• gnomAD v3: 7-107672114-T-C
• gnomAD v4: 7-107672114-T-C
• MyVariant Identifiers: chr7:g.107312559T>C (hg19) ; chr7:g.107672114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107672114T>C , CM000669.2:g.107672114T>C	GRCh38
NC_000007.13:g.107312559T>C , CM000669.1:g.107312559T>C	GRCh37
NC_000007.12:g.107099795T>C	NCBI36
NG_008489.1:g.16480T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.305-24T>C MANE Select	ENSP00000494017.1:n.305-24T>C
ENST00000265715.7:c.305-24T>C	ENSP00000265715.3:n.305-24T>C
ENST00000440056.1:c.305-24T>C	ENSP00000394760.1:n.305-24T>C
NM_000441.1:c.305-24T>C	NP_000432.1:n.305-24T>C
XM_005250425.1:c.305-24T>C	XP_005250482.1:n.305-24T>C
XM_006716025.2:c.305-24T>C	XP_006716088.1:n.305-24T>C
XM_005250425.2:c.305-24T>C	XP_005250482.1:n.305-24T>C
XM_006716025.3:c.305-24T>C	XP_006716088.1:n.305-24T>C
XM_017012318.1:c.305-24T>C	XP_016867807.1:n.305-24T>C
NM_000441.2:c.305-24T>C MANE Select	NP_000432.1:n.305-24T>C