Canonical Allele Identifier: CA99701508

Gene: ALB

Linked Data

• dbSNP Id: rs75828235
• MyVariant Identifiers: chr4:g.74275205G>C (hg19) ; chr4:g.73409488G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409488G>C , CM000666.2:g.73409488G>C	GRCh38
NC_000004.11:g.74275205G>C , CM000666.1:g.74275205G>C	GRCh37
NC_000004.10:g.74494069G>C	NCBI36
NG_009291.1:g.10234G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.615+1G>C MANE Select	ENSP00000295897.4:n.615+1G>C
ENST00000295897.8:c.615+1G>C	ENSP00000295897.4:n.615+1G>C
ENST00000401494.7:c.270+1G>C	ENSP00000384695.3:n.270+1G>C
ENST00000415165.6:c.138-2508G>C	ENSP00000401820.2:n.138-2508G>C
ENST00000476441.6:c.212+1G>C	ENSP00000423727.1:n.212+1G>C
ENST00000503124.5:c.165+1G>C	ENSP00000421027.1:n.165+1G>C
ENST00000505649.5:n.301+1G>C
ENST00000509063.5:c.615+1G>C	ENSP00000422784.1:n.615+1G>C
ENST00000511370.1:c.148+1G>C
ENST00000621085.4:c.490+126G>C	ENSP00000483421.1:n.490+126G>C
ENST00000621628.4:c.486+412G>C	ENSP00000480485.1:n.486+412G>C
NM_000477.5:c.615+1G>C	NP_000468.1:n.615+1G>C
NM_000477.6:c.615+1G>C	NP_000468.1:n.615+1G>C
NM_000477.7:c.615+1G>C MANE Select	NP_000468.1:n.615+1G>C