Canonical Allele Identifier: CA703265647

Gene: AMN

Linked Data

• dbSNP Id: rs1382534909
• MyVariant Identifiers: chr14:g.103394666G>C (hg19) ; chr14:g.102928329G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102928329G>C , CM000676.2:g.102928329G>C	GRCh38
NC_000014.8:g.103394666G>C , CM000676.1:g.103394666G>C	GRCh37
NC_000014.7:g.102464419G>C	NCBI36
NG_008276.2:g.10674G>C , LRG_642:g.10674G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299155.10:c.208-97G>C MANE Select	ENSP00000299155.6:n.208-97G>C
ENST00000299155.9:c.208-97G>C	ENSP00000299155.5:n.208-97G>C
ENST00000541086.5:n.954-97G>C
NM_030943.3:c.208-97G>C , LRG_642t1:c.208-97G>C	NP_112205.2:n.208-97G>C
XM_011537202.1:c.46-97G>C	XP_011535504.1:n.46-97G>C
XM_011537203.1:c.46-97G>C	XP_011535505.1:n.46-97G>C
XM_011537202.3:c.46-97G>C	XP_011535504.1:n.46-97G>C
XM_011537203.3:c.46-97G>C	XP_011535505.1:n.46-97G>C
XM_024449714.1:c.304-97G>C	XP_024305482.1:n.304-97G>C
NM_030943.4:c.208-97G>C MANE Select	NP_112205.2:n.208-97G>C